Dissertations / Theses on the topic 'Clinic reports'
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Plews, Caroline Margaret Coatsworth. "Clients' reports of the work of health visitors in the child health clinic and during home visits." Thesis, University of Hull, 2001. http://hydra.hull.ac.uk/resources/hull:4626.
Full textRandmaa, Maria. "Communication and Patient Safety : Transfer of information between healthcare personnel in anaesthetic clinics." Doctoral thesis, Uppsala universitet, Institutionen för folkhälso- och vårdvetenskap, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-278726.
Full textMolloy, Mari. "Research projects reports and professional and ethical issues report." Thesis, The Author [Mt. Helen, Vic.] :, 2004. http://researchonline.federation.edu.au/vital/access/HandleResolver/1959.17/40390.
Full textMeagher, Brendan University of Ballarat. "Clinical placement reports and professional and ethical issues reports." University of Ballarat, 2006. http://archimedes.ballarat.edu.au:8080/vital/access/HandleResolver/1959.17/12760.
Full textDoctor of Psychology (Clinical)
Meagher, Brendan. "Clinical placement reports and professional and ethical issues reports." University of Ballarat, 2006. http://archimedes.ballarat.edu.au:8080/vital/access/HandleResolver/1959.17/14595.
Full textDoctor of Psychology (Clinical)
Mackenzie, Tania. "Reported responses to sexual trauma in people with intellectual disability : an analysis of clinical psychologists' psycho-legal reports." Master's thesis, University of Cape Town, 2010. http://hdl.handle.net/11427/18425.
Full textMoniz, Jennifer Lela. "Confusing Conversations: Assessing Traumatic Stress in Young Children." Antioch University / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=antioch1587067693985147.
Full textHawker, Mark David. "Health Watch : a management tool combining clinical and population data sets /." Leeds : University of Leeds, School of Computer Studies, 2008. http://www.comp.leeds.ac.uk/fyproj/reports/0708/Hawker.pdf.
Full textTinker, Jennifer Ruby Zillmer Eric. "Reported visual disturbance and post-concussion cognitive function in collegiate athletes : the relationship between symptom report and neurocognitive outcome /." Philadelphia, Pa. : Drexel University, 2010. http://hdl.handle.net/1860/3264.
Full textChung, Jeanhee 1972. "Concept-value pair extraction from semi-structured clinical reports : a case study using echocardiogram reports." Thesis, Massachusetts Institute of Technology, 2004. http://hdl.handle.net/1721.1/28584.
Full textIncludes bibliographical references (p. 38-39).
The task of gathering detailed patient information from narrative clinical text presents a significant barrier to clinical research. A prototype information extraction system was developed to extract pre-specified findings from narrative echocardiogram reports. The system which uses a Unified Medical Language System compatible architecture is very simple and takes advantage of canonical language use patterns to identify sentence templates with which concepts and their values can be identified. The data extracted from this system will be used to enrich an existing database used by clinical researchers in a large university healthcare system to identify potential research candidates fulfilling clinical inclusion criteria. The system was developed and evaluated using ten pre-determined clinical concepts. Concept-value pairs extracted by the system related to these ten conditions were compared with findings extracted manually by the author. The system was able to recall 78% of the relevant findings (CI, 76% to 80%), with a precision of 99% (CI, 98%-99%). Because data acquired from the system will ultimately be used in document and patient retrieval, preliminary analysis was done to evaluate document retrieval effectiveness. Median recall across the ten conditions was 36% (range, 0% to 93%). The system retrieved no documents for two of the ten conditions; median precision for the remaining eight conditions was 100% (range, 92% to 100%).
by Jeanhee Chung.
S.M.
Lindblad, Simon. "Labeling Clinical Reports with Active Learning and Topic Modeling." Thesis, Linköpings universitet, Interaktiva och kognitiva system, 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-148463.
Full textOliveira, Liliana Cristina Santos. "Curricular training report about clinical trials monitoring." Master's thesis, Universidade de Aveiro, 2012. http://hdl.handle.net/10773/10578.
Full textO presente relatório propõe-se a apresentar as atividades desenvolvidas durante um estágio curricular de 10 meses na Datamedica CRO Full Service. A estagiária encontrava-se a desenvolver atividades de monitorização de ensaios clínicos na empresa recetora pelo que este será o principal enfoque deste trabalho. Após 6 meses de estágio curricular, a Astellas Farma Lda subcontratou à Datamedica a estagiária em questão para desempenhar a função de CRA o que permitiu conhecer o mundo dos ensaios clínicos de duas diferentes perspetivas - a das grandes empresas da indústria farmacêutica e a das CROs (empresas subcontratadas pela indústria farmacêutica para desenvolver atividades específicas). Este trabalho tenta mostrar a visão obtida e os pontos de vista da estagiária enquanto monitora de ensaios clínicos das duas empresas. Para além da monitorização, foi possível desenvolver outras atividades em outros departamentos da Datamedica, nomeadamente realização de testes de legibilidade e atividades de medical writing que serão também apresentadas neste relatório. Este trabalho encontra-se dividido em dois principais capítulos sendo que o primeiro capítulo pretende situar a empresa de acolhimento na dinâmica da investigação clínica farmacêutica e dar a conhecer o estado da arte dos ensaios clínicos a nível europeu e nacional, com ênfase para a crise na investigação clínica em ambos os níveis. O segundo capítulo constitui a apresentação dos procedimentos que são seguidos em cada área de trabalho desenvolvida durante o período de estágio e a identificação de todas as atividades realizadas pela estagiária. O relatório termina com a discussão e conclusão de todo o trabalho desenvolvido e verificação dos objetivos de aprendizagem definidos no início do estágio. Todo o trabalho desenvolvido durante o estágio curricular e o contacto com os diversos profissionais envolvidos na área da investigação clínica foram fundamentais para a aquisição de competências sociais e intelectuais que contribuíram para o melhor desempenho da estagiária e a prepararam para o mundo profissional da indústria farmacêutica.
This paper intends to present the activities developed during a 10-month internship at Datamedica Full Service CRO. The trainee was developing clinical trial monitoring activities at the host company, which will be the main focus of this report. After 6 months of internship, Astellas Farma Lda subcontracted the trainee from Datamedica to be one of their CRA’s, providing her with an opportunity to experience the world of clinical trials from two different perspectives - the major pharmaceutical companies and the CROs (companies subcontracted by the pharmaceutical industry to develop specific activities). This report tries to show the point of view of the trainee as clinical trial monitor of the two companies. Besides clinical trial monitoring it was possible to develop different activities from other Datamedica departments such as the realization of readability tests and medical writing activities that will also be presented in this report. This paper is divided in two main chapters, where the first chapter goal is to place the host company dynamics in the pharmaceutical clinical research environment and provide some knowledge about the clinical trials state of the art nationally and internationally, highlighting the clinical research crisis that is threatening the pharmaceutical world at both levels. The second chapter presents the procedures followed with the different activities performed divided by area of work and the identification/specification of each activity developed by the trainee. The report ends with a discussion and conclusion about the work developed and the verification of the learning outcomes defined at the beginning of the internship. The work developed during this curricular internship and the contact network developed through the contact with a variety of professionals involved in the clinical research area were essential in the acquisition of social and intellectual skills that contributed to the best performance of the trainee during the internship and prepared her to the professional work environment of the pharmaceutical industry.
Simas, Ana Luísa Oliveira de. "Training report : clinical studies coordination in oncology." Master's thesis, Universidade de Aveiro, 2014. http://hdl.handle.net/10773/12966.
Full textThis report describes a curricular training experience in Study Coordination, developed at Unidade de Investigação Clínica (Clinical Research Unit) of Instituto Português de Oncologia do Porto Francisco Gentil, E.P.E. (Portuguese Oncology Institute-Porto), in the ambit of the Master in Pharmaceutical Medicine at University of Aveiro. This report describes the State of the Art in Pharmaceutical R&D Process in Europe, especially in Oncology, emphasising its current trends and stressing specificities of special and vulnerable populations, in the scope of the traineeship. The study coordination activities were essentially performed in the Pathology Clinics of Lung, Urology, Gynaecology, Paediatrics, and the Intensive Care Service. The activities developed had the main goal of acquiring experience in oncology clinical trials, while reinforcing the knowledge from my academic background. These activities included screening and randomisation of patients, preparation and processing of study visits, data entry and query resolution, and documents management, among other activities transversal to the 15 clinical trials, accompanied in the traineeship. Globally, the traineeship allowed a good overview of the activities involved in the conduction of clinical trials in a hospital, and a worthy introduction to the marketplace. I strengthened the knowledge acquired from my academic background. I developed competences and skills at the professional and personal level, such as dealing with unforeseen situations, and developed strategies to overcome challenges. I sharpened my vision of careers in clinical research, and hope to continue addressing new challenges in this area.
Alves, André Ribeiro. "Curricular training report in clinical data management." Master's thesis, Universidade de Aveiro, 2013. http://hdl.handle.net/10773/10875.
Full textEste relatório descreve as actividades desenvolvidas no contexto do estágio de 9 meses realizado na Unidade de Gestão de dados da Eurotrials com inicio em Setembro de 2011 e fim em Maio de 2012. A Eurotrials é uma empresa de consultoria científica que presta serviços à indústria farmacêutica e biotecnologia, nomeadamente na condução de ensaios clínicos. No processo do desenvolvimento de um novo medicamento os ensaios clínicos são a ferramenta mais importante de forma a verificar a segurança e eficácia da substância. A gestão de dados cínicos tem um papel muito importante na condução de ensaios clínicos e tem como objectivo gerar dados de grande qualidade e robustos para que possam ser analisados. A equipa de gestão de dados participa em actividades que vão desde o planeamento do estudo até à sua conclusão. As principais actividades exercidas no âmbito da gestão de dados foram o desenho do caderno de recolha de dados, bem como a criação da base de dados, gestão de discrepâncias e padronização de dados.
This report describes the activities undertaken in the context of a Curricular training with a duration of 9 months in the Data Management Unit at Eurotrials starting in September 2011 and end in May 2012. Eurotrials is a contract research organization that provides services to the pharmaceutical and biotechnology industries, namely clinical trial conduction. In the drug development process, clinical trials are the most important tool to verify if the drug is secure and effective. The field of clinical data management has a very important role in clinical trials conduction and aims to generate high-quality and reliable data so that it can be analyzed. The data management team is engaged in activities ranging from the design of the study until their completion. The main activates performed regarding clinical data management were the design of the case report form, database design, discrepancies management and data standardization.
Morais, Catarina Manuel Souto. "Curricular training report at Blueclinical Ltd." Master's thesis, Universidade de Aveiro, 2014. http://hdl.handle.net/10773/13399.
Full textThis report describes the activities I have developed and the knowledge I have acquired during my curricular training as Clinical Research Coordinator at Blueclinical – Investigação e Desenvolvimento em Saúde, Ltd. The curricular training is part of the second year of the Master’s Degree program in Pharmaceutical Biomedicine University of Aveiro. The main activity developed was the clinical trials coordination at Hospitalar Center Vila Nova de Gaia/Espinho, since the earliest phases – feasibilities – until latest phases – close-out visit. Nevertheless being part of a recent company, still in creation phase, was a positive aspect as it allowed me to perform a large variety of tasks, including management, creation of the quality system, among others. During the internship I was able to acknowledge the difficulties faced while creating and implementing a clinical research office, as well as acknowledge some differences between the academic environment and the professional environment. Besides the description of the activities developed and the objectives, this reports intents to contextualize the internship in Blueclinical’s structure and in clinical research state of art. It is also presented a critical analysis of the strengths, weakness, opportunities and threats faced during the curricular training.
Este relatório descreve as atividades que desenvolvi e as aprendizagens que adquiri durante o meu estágio curricular, enquanto Coordenadora de Investigação Clínica na Blueclinical – Investigação e Desenvolvimento em Saúde, Lda. O estágio curricular foi realizado no âmbito do segundo ano do Mestrado de Biomedicina Farmacêutica da Universidade de Aveiro. A principal atividade desenvolvida foi a coordenação de ensaios clínicos no Centro Hospitalar Vila Nova de Gaia/Espinho, desde as fases mais iniciais do seu desenvolvimento – questionários de exequibilidade – até às fases mais tardias – visita de fecho. No entanto, pertencer a uma empresa ainda em processo de criação foi uma mais-valia pela pluralidade das tarefas efetuadas, incluindo tarefas relacionadas com gestão, criação do sistema de gestão de qualidade, entre outras. Durante o estágio foi-me possível tomar conhecimento das dificuldades encontradas durante a criação e implementação de um Gabinete de Investigação Clínica e também aperceber-me de algumas diferenças entre o mundo académico e o mundo profissional. Para além da descrição das atividades desenvolvidas e dos objetivos que me propôs a atingir, este relatório tenta contextualizar o estágio na estrutura da Blueclinical e no estado de arte da investigação clinica. É também apresentada uma análise crítica dos pontos fortes, pontos fracos, dificuldades e oportunidades encontrados durante o estágio.
Granja, Joana Fernanda Durães Barbosa. "Curricular training report at Blueclinical, LTD." Master's thesis, Universidade de Aveiro, 2015. http://hdl.handle.net/10773/23514.
Full textO presente relatório descreve com detalhe o meu período de estágio curricular realizado durante o Mestrado em Biomedicina Farmacêutica. O estágio teve a duração de 9 meses e ocorreu na Blueclinical Lda., uma empresa constituída por três unidades de negócio distintas: Unidade de Fase I, Unidade de Investigação e Desenvolvimento e uma Unidade de Parceria com Centros de Ensaio - Clinical Research Partnership (CRP). A minha atividade foi desenvolvida apenas numa unidade de negócio – CRP. No entanto tive oportunidade de conhecer duas realidades distintas, exercendo funções num centro de ensaio como coordenadora de ensaios clínicos e funções na Blueclinical Back Office, com funções de apoio à unidade CRP, essencialmente na gestão de contratos financeiros e pagamentos. Neste relatório é revisto o estado de arte da investigação clínica e são descritas as principais atividades realizadas durante o estágio. São igualmente relatadas, as principais dificuldades sentidas, as estratégias utilizadas para as ultrapassar e objetivos que considero alcançados. A realização deste estágio foi uma excelente oportunidade que me permitiu consolidar os conteúdos teóricos adquiridos durante o primeiro ano do mestrado, obtendo a experiência necessária para ingressar no mundo de trabalho da Investigação Clínica.
The present report describes in detail my internship period, during the Master in Pharmaceutical Medicine. The internship lasted 9 months and was performed in Blueclinical Ltd., a company that has three business units: Phase I Unit, Research and Development Unit and Clinical Research Partnership Unit (CRP). My activities were performed in only one business unit - CRP, however I had the opportunity to experience two different realities, exercising functions as Clinical Research Coordinator at site and support functions at Blueclinical Back office, mainly contract management and payment tracking. This report reviews state of art of clinical research and describes main activities performed during internship. Along with the description of the activities performed, it is done a presentation of the difficulties encountered, strategies used to overcome them and objectives I considered achieved. This internship was a great opportunity that allowed me to consolidate theoretical knowledge acquired during the first year of the master, giving me the necessary experience to cross into Clinical Research job market
Plunkett, Alicia Renee'. "The Use of a Standardized System of Communication to Change the Perception of Handoff Communication in a Psychiatric Setting." ScholarWorks, 2015. https://scholarworks.waldenu.edu/dissertations/200.
Full textSantos, Ana Teresa Martins Sousa. "Report on training in a clinical research centre." Master's thesis, Universidade de Aveiro, 2012. http://hdl.handle.net/10773/10486.
Full textA crescente exigência de pesquisa científica, das agências reguladoras e a necessidade de maximizar a segurança dos participantes têm requerido uma gestão mais eficiente, capaz e precisa para realizar estudos de alta qualidade de pesquisa clínica e melhorar a competitividade neste campo. Para enfrentar este desafio, centros de pesquisa clínica tem surgido para apoiar os requisitos operacionais, metodológicos e regulamentares. Este trabalho relata a minha experiência de Setembro 2011 a Junho de 2012 num centro de investigação clínica como coordenadora e co-monitora de ensaios clínicos e estudos observacionais na Unidade Neurológica de Investigação Clínica do Instituto de Medicina Molecular, as atividades de farmacovigilância realizados numa unidade regional do Sistema de Farmacovigilância Português e as tarefas de gestão científica desenvolvidas envolvendo estas duas unidades. Como um estágio curricular com objetivo de colocar em prática os conceitos aprendidos no primeiro ano de mestrado em Biomedicina Farmacêutica, tive a oportunidade de experimentar diferentes papéis ligados à investigação clínica e compreender as responsabilidades e expectativas envolvidas em cada um deles. Este estágio curricular deu-me uma visão realista de um centro de investigação clínica, bem como as interações entre os diferentes profissionais.
The growing demand of scientific research, regulatory agencies and the need to maximize participant safety have required efficient, capable and precise management to conduct high-quality clinical research studies and improve the competitiveness in this field. To face up to this challenge, clinical research centers have emerged to support the operational, methodological and regulatory requirements. This work reports on my experience since September 2011 until June 2012 in a clinical research centre coordinating and monitoring the clinical trials in the Neurological Clinical Research Unit of Instituto de Medicina Molecular, the Pharmacovigilance activities performed in a regional unit of the Portuguese Pharmacovigilance System and the Science Management tasks developed involving these two units. As a curricular internship aimed to put into practice the concepts learnt in the first year of master’s degree in Pharmaceutical Biomedicine, I had the opportunity to experience different roles linked to the clinical research and realize the responsibilities and expectations involved in each one of them. This curricular training provided a realistic vision of a clinical research center as well as the interactions between different professionals.
Ferreira, Adriana Filipa da Silva. "Curricular training report: clinical trials coordination in neurology." Master's thesis, Universidade de Aveiro, 2015. http://hdl.handle.net/10773/21557.
Full textO presente relatório descreve as atividades desenvolvidas durante o estágio curricular como coordenadora de investigação clínica, que teve lugar na Unidade de Farmacologia Clínica do Instituto de Medicina Molecular e decorreu de Setembro de 2014 a Junho de 2015. A principal atividade desempenhada durante este estágio foi a coordenação de ensaios clínicos na área da neurologia, nomeadamente ensaios de fase II, III e IV. Foram desenvolvidas outras atividades, tais como gestão de dados clínicos, atividades de farmacovigilância e escrita científica e monitorização de estudos clínicos, com vista a complementar a formação curricular. Neste relatório é, também, apresentada uma breve contextualização do estado de arte do processo de Investigação & Desenvolvimento de novos medicamentos, tendências atuais e especificidades do desenvolvimento de medicamentos na área da neurologia. Para além disso são abordadas as dificuldades sentidas durante o estágio e as estratégias utilizadas para as ultrapassar, bem como a visão pessoal sobre o papel do coordenador de investigação clínica na condução de ensaios clínicos. Globalmente, a realização deste estágio curricular traduziu-se na oportunidade de aplicar e aprofundar os conhecimentos e competências adquiridos ao longo do percurso académico, em especial no Mestrado em Biomedicina Farmacêutica, e de desenvolver competências e aptidões, tanto a nível profissional como pessoal, fulcrais para um profissional de investigação clínica. Em conclusão, este estágio constituiu uma introdução à prática da investigação clínica.
This report describes the activities developed during the curricular training as coordinator of clinical research, which took place in the Unidade de Farmacologia Clínica of the Instituto de Medicina Molecular and was held from September 2014 to June 2015. The main activity performed during this training was the coordination of clinical trials in the field of neurology, mainly phase II, III and IV clinical trials. Other activities, such as data management, pharmacovigilance, medical writing and monitoring of clinical studies, were developed to complement the training. This report also presents a brief background of the state of the art of the Research & Development process of new drugs, current trends and specificities of the drug development in neurology. Furthermore, it addresses the difficulties experienced during the training and the strategies used to overcome them, as well as a personal insight on the role of the clinical research coordinator in conducting clinical trials. Overall, achieving this curricular training resulted in the opportunity to apply and deepen the knowledge and skills acquired throughout the academic career, especially in the Masters in Pharmaceutical Biomedicine, and to develop skills and abilities, at professional and personal level, central to a professional of clinical research. In conclusion, this training was an introduction to the practice of clinical research.
Swaminathan, Sindhia. "Relationships between symptoms and adaptive functioning in clinic-referred adolescents: Patterns of internalizing, externalizing, and co-occurring symptoms." Bowling Green State University / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1457534784.
Full textCorreia, Márcia Sofia Barbosa. "Internship report in clinical studies coordination at IPO-Porto." Master's thesis, Universidade de Aveiro, 2014. http://hdl.handle.net/10773/12949.
Full textThis report describes my activities as study coordinator (SC) intern, at the “Unidade de Investigação Clínica” (UIC) in the Oncology Portuguese Institute of Porto (IPOP). This training occurred during the second year of the Pharmaceutical Biomedicine Master at the University of Aveiro. My internship took place between 21st January, 2013 and 4th October, 2013 with the main objective to gain experience and expertise in oncology coordinating clinical trials. I present the state-of-the-art of clinical research with emphasis on current situation in Portugal as well as in oncology. At the beginning of internship I performed generic training in Good Clinical Practices (GCP) and Electronic Data Capture systems and familiarised myself with terminology and classification/assessment systems regarding the oncology area to support the clinical trial coordination activities in the context of the oncology protocols. In UIC, I participated in 6 phase II and 25 phase III clinical trials of 9 clinics of pathology: Urology, Gynaecology, Digestive, Lung, Soft Tissue and Skin, Head and Neck, Onco-Haematology, Breast and Paediatry. Within of these clinics, I intensively participated and acquired more autonomy in clinical trials of the Digestive pathology. The Onco-Haematology clinic includes the more complex procedures of the clinical trials protocols. As SC, I could intensively participate in the conduction clinical trial activities, namely: Randomisation Period, including Screening and Randomisation of patients, Clinic Visits and Monitoring Visits. The experience gained during my curricular internship was very enriching and enabled me to acquire professional and interpersonal skills and competences and to face unexpected situations, developing strategies to deal with them. Additionally, it was possible to consolidate and apply the theoretical knowledge acquired during Master Course in Pharmaceutical Medicine at different stages of clinical trials coordination. In conclusion, during my curricular internship, I gathered the competences, motivation and experience to pursue a career in clinical research, particularly, as SC.
Este relatório descreve as actividades como coordenadora de estudos estagiária, na Unidade de Investigação Clínica (UIC) do Instituto Português de Oncologia do Porto (IPOP). Este estágio foi parte integrante das actividades curriculares do segundo ano do Mestrado em Biomedicina Farmacêutica da Universidade de Aveiro. O estágio decorreu entre 21 de Janeiro de 2013 e 4 de Outubro de 2013, com o principal objectivo em adquirir experiência e especialização na coordenação de ensaios clínicos em oncologia. No documento é apresentado o estado de arte de arte da investigação clínica com ênfase na actual situação em Portugal bem como em oncologia. Na fase inicial do estágio realizei treino genérico em Boas Práticas Clínicas e sistemas de Captura de Dados Electrónicos e familiarizei-me com terminologia e sistemas classificação/avaliação próprios da área de oncologia para suportar as actividades de coordenação de ensaios clínicos no contexto dos protocolos de oncologia. Na UIC, participei em vários estudos de fase II e III de 9 clínicas de patologia: Urologia, Ginecologia, Digestivos, Pulmão, Pele e Tecidos Moles, Cabeça e Pescoço, Onco-Hematologia, Mama e Pediatria. Dentro destas clínicas, participei intensivamente e adquiri mais autonomia nos ensaios clínicos da patologia de Digestivos. A clínica de Onco-Hematologia, agrega os protocolos de ensaios clínicos com procedimentos mais complexos. Como coordenadora de ensaios clínicos pude participar intensivamente nas actividades de condução de um ensaio clínico, nomeadamente: Período de Randomização incluindo Rastreio e Randomização de doentes, Visitas Clínicas e Visitas de Monitorização. A experiência adquirida ao longo do estágio curricular foi muito enriquecedora e permitiu-me adquirir capacidades e competências profissionais e interpessoais e aprender a enfrentar situações inesperadas, desenvolvendo estratégias para lidar com as mesmas. Para além disso possibilitou-me a consolidar e aplicar os conhecimentos teóricos adquiridos no Curso de Mestrado nas diferentes fases de coordenação dos estudos. Em conclusão, ao longo do estágio adquiri competências, motivação e experiência para enveredar por uma carreira na área de investigação clínica, especialmente como Coordenadora de Ensaios Clínicos.
Lemos, João Filipe Carvalho. "Internship report as associated project manager at Blueclinical." Master's thesis, Universidade de Aveiro, 2013. http://hdl.handle.net/10773/13133.
Full textThe present curricular report describes the activities that I performed as an associate project manager at Blueclinical, Lda a portuguese company that develops its activities in the research and development of health’s. As I mostly worked with medical devices, in this report there is a brief review of the state of the art about this area giving emphasis to the portuguese case. During the 9 months of the internship, I had the opportunity of completing my academic formation with some training and training which are mentioned. Concerning the specific training, the activities related to the medical devices area and phase I clinical studies are described as well as the activities that I performed as a clinical study coordinator. Additionally, there are other activities mentioned, such as SOP’s writing and the study of QREN legislation. Following that, there is a final discussion about the difficulties felt and what was learnt during the internship. The report ends with a conclusion/reflexion about this curricular internship.
Este relatório de estágio descreve as atividades que desenvolvi enquanto gestor de projeto associado na Blueclinical, Ltd, companhia portuguesa que desenvolve atividade na Investigação e desenvolvimento na saúde. Como a minha principal área de trabalho foram os dispositivos médicos, este relatório faz uma curta revisão do estado da arte nesta área com enfâse no caso português. Nos 9 meses de estágio, tive a oportunidade de completar a minha formação com algumas formações e treinos, que são também referidos. Na formação específica, são descritas as atividades relacionadas com a área dos dispositivos médicos, com os ensaios clínicos de fase I e as atividades como coordenador de estudos clínicos. Para além destas também são referidas outras atividades como por exemplo a escrita de SOPs, ou o estudo da legislação do QREN. Segue-se uma discussão geral sobre as dificuldades sentidas e o que aprendi durantes este período. O relatório termina com uma conclusão/reflexão sobre este estágio curricular.
Sousa, Joana Cristina Mendes Cruz de. "Training report in clinical trials coordination at Blueclinical, LTD." Master's thesis, Universidade de Aveiro, 2016. http://hdl.handle.net/10773/17158.
Full textThis report describes the activities performed as clinical research coordinator, during the internship of the Master in Pharmaceutical Medicine, at the University of Aveiro. The curricular internship took place at Blueclinical – particularly at Centro Hospitalar de Vila Nova de Gaia/Espinho, from 15th September 2015 to 15th April 2016. The report is divided into seven chapters. The training objectives are presented in the two chapter, and in the next chapter the host institutions are characterized. Then, in the four chapter it is presented the state-of-the-art of the pharmaceutical research and development process, including the current situation of the clinical trials in Portugal. The activities carried out under the scope of the clinical trials coordination are described in five four. In the last chapters, it is performed a critical analysis and the assessment of the internship, and are also mentioned the strategies adopted in order to solve the problems and difficulties that arose. In conclusion, I consider that the internship fulfilled its purpose, providing the acquisition of skills as clinical research coordinator.
Este relatório descreve as atividades desenvolvidas como coordenadora de ensaios clínicos no âmbito do estágio curricular do Mestrado em Biomedicina Farmacêutica, lecionado na Universidade de Aveiro. O estágio curricular decorreu no Centro Hospitalar de Vila Nova de Gaia/Espinho, no período compreendido entre 15 de setembro de 2015 e 15 de abril de 2016. O relatório encontra-se estruturado em sete capítulos, sendo que no segundo capítulo são mencionados os objetivos do estágio, procedendo-se no capítulo seguinte à caracterização das instituições acolhedoras. Posteriormente, no capítulo quatro é apresentado o estado de arte do processo de investigação e desenvolvimento farmacêutico, incluindo a caraterização da situação atual dos ensaios clínicos em Portugal. As atividades realizadas no âmbito da coordenação de ensaios clínicos estão descritas no capítulo cinco. Nos últimos capítulos, analisa-se e procede-se à avaliação do estágio, sendo também mencionadas as estratégias adotadas para solucionar os problemas e dificuldades que foram surgindo. Em suma, considero que o estágio curricular cumpriu a sua finalidade, ao possibilitar a aquisição de competências como coordenadora de investigação clínica.
VIANI, NATALIA. "Information Extraction from Medical Reports in the Italian Language for Clinical Timelines Reconstruction." Doctoral thesis, Università degli studi di Pavia, 2018. http://hdl.handle.net/11571/1214892.
Full textValente, Vanessa Sofia Silva. "Curricular training report as a clinical research coordinator in Blueclinical Ltd." Master's thesis, Universidade de Aveiro, 2016. http://hdl.handle.net/10773/16505.
Full textThis report describes the activities developed within the curricular internship as a clinical research coordinator in the Clinical Research Partnership business area of Blueclinical. The internship lasted 10 months – from July 2014 until April 2015. This report provides a general view of the implementation of clinical trials and observational studies in clinical research centers alongside with my experience during the 10 months of curricular internship as a clinical research coordinator in Centro Hospitalar de Vila Nova de Gaia/Espinho. To understand the regulations under which my activities were developed, clinical research is contextualized in what regards it’s legal and ethical framework and the evolution of the number of clinical trials in Portugal along the last years. In the overall result, I have experienced a great improvement in understanding the coordination of clinical trials and observational studies, as well as the improvement of my soft skills.
O presente relatório descreve as atividades desenvolvidas no âmbito do estágio curricular como coordenadora de investigação clínica na área de negócio “Clinical Research Partnership” da Blueclinical. O estágio curricular teve a duração de 10 meses – Julho de 2014 a Abril de 2015. Este relatório fornece uma visão geral da implementação de ensaios clínicos e estudos observacionais em centros de investigação clínica em paralelo com a minha experiência durante os 10 meses de estágio curricular como coordenadora de investigação clínica no Centro Hospitalar de Vila Nova de Gaia/Espinho. Para permitir a compreensão das normas segundo as quais a minha atividade foi desenvolvida, é feita uma contextualização da investigação clínica no que respeita ao enquadramento legal, ético e evolução do número de ensaios em Portugal ao longo dos últimos anos. No cômputo geral, experimentei uma grande melhoria na compreensão da coordenação de ensaios clínicos e estudos observacionais, assim como a nível de “soft skills”.
TOMODA, YUTAKA, HIROSHI SAKAIDA, SETSUKO GOTO, SEIJI NOMURA, TORU NAKANISHI, and TOMOMITSU OKAMOTO. "An Unusual Clinical Course after Mole Evacuation: A Case Report." Nagoya University School of Medicine, 1997. http://hdl.handle.net/2237/16752.
Full textRozhko, V. I. "Case report: clinical result of revascularization of a permanent tooth." Thesis, БДМУ, 2021. http://dspace.bsmu.edu.ua:8080/xmlui/handle/123456789/19129.
Full textAraújo, Isabel Cristina Fontes Almeida Sousa. "Report of training in clinical trials coordination in a hospital." Master's thesis, Universidade de Aveiro, 2012. http://hdl.handle.net/10773/10585.
Full textEste relatório descreve as minhas actividades como coordenadora de estudos estagiária, durante 9 meses, no serviço de neurologia do Centro Hospitalar de Entre o Douro e Vouga, em Santa Maria da Feira. Este estágio foi parte integrante das actividades curriculares do segundo ano do Mestrado em Biomedicina Farmacêutica da Universidade de Aveiro. Este estágio permitiu-me desenvolver capacidades de coordenação de ensaios clínicos e estudos observacionais, bem como outras actividades de investigação desenvolvidas, incluindo preenchimento de bases de dados de estudos nacionais e internacionais, participação em projectos de longa duração e artigos científicos. Para além destas actividades, tive também a oportunidade de participar na validação de um questionário de qualidade de vida para a população portuguesa que sofre de Hipertensão Pulmonar, no Hospital de Santo António, no Porto. Os conhecimentos adquiridos ao longo de todo o meu percurso académico (licenciatura em Ciências Biomédicas e Mestrado em Biomedicina Farmacêutica) foram extremamente úteis para o desenvolvimento das actividades que me foram propostas e a integração no mercado do trabalho.
This report describes my activities as study coordinator intern, during nine months, in the neurology service of Centro Hospitalar de Entre o Douro e Vouga, in Santa Maria da Feira. This training occurred during the second year of the Pharmaceutical Biomedicine Master at the University of Aveiro. This training allowed me develop abilities in coordination of clinical trials and observational studies, as well as perform other research activities developed in the neurology service, including filling in of national and international databases of studies, participation in long duration projects and scientific articles. Beyond that, I also had the opportunity to participate in the validation of a quality of life questionnaire for Portuguese population with pulmonary arterial hypertension, in the Hospital Santo António, Porto. My background knowledge was useful to develop the activities proposed in the training and to my integration in the working market.
Merikle, Elizabeth Paige 1965. "Development of a self-report measure of drug craving." Diss., The University of Arizona, 1997. http://hdl.handle.net/10150/289233.
Full textZelechoski, Amanda Dovidio Goldstein Naomi E. Sevin. "The content of child custody evaluation reports: a forensic assessment principles-based analysis /." Philadelphia, Pa. : Drexel University, 2009. http://hdl.handle.net/1860/3025.
Full textVallabh, Sheetal. "Towards being heard : representations of the child's voice in custody evaluation reports by the Family Advocate's Office." Master's thesis, University of Cape Town, 2009. http://hdl.handle.net/11427/14061.
Full textThis study outlined the changing social and legal contexts insofar as it relates to children's participation in matters that affect their lives. It set out the debates in the literature on whether not children should participate in family law matters, specifically custody disputes, and if so, how this participation should take place. It also drew upon research studies which have explored directly children's views on the issue. The challenges involved in custody evaluations were scrutinised, specifically in relation to the Family Advocate's Office, and alternative and/or complementary methods of accessing the child's voice were considered. In South Africa, in all access and/or custody disputes, the Family Advocate’s Office is tasked with making recommendations to the court, which are in the child's best interest. The recently promulgated provisions of the Children's Act (2005) also require that the child's views and wishes be taken into consideration. Accordingly, this research study involved a thematic content analysis of 10 Family Counsellor reports, in order to determine how the child's voice is accessed by the Family Advocate's Office. A structural model illustrating how the child's voice was represented in the reports was developed. It showed that the child's voice was represented in three distinct ways, namely: the child's voice is accessed directly; the child's voice is disqualified; and the archetypal child's voice is accessed through a proxy. The findings showed a tendency to rely more on accessing the archetypal child's voice through a proxy, which typically included reporting that was less descriptive and more inferential, interpretive and opinion-laden. A need for more direct, non-disqualified means of accessing and/or reporting on the child's views and wishes was indicated.
Moreira, Paula Cristina Leão. "Internship report on Blueclinical phase I unit." Master's thesis, Universidade de Aveiro, 2014. http://hdl.handle.net/10773/13413.
Full textBioavailability/Bioequivalence clinical trials are a promising area in Pharmaceutical R&D and it is very interesting being involved in this field. During the internship, I practiced assistance activities to Bioavailability/Bioequivalence clinical trials and this was my target for intervention within Blueclinical during ten months. During this time I also had opportunity to exercise nursing research activities due to my previous training in the area. This report aims to describe the activities in which I was involved, the learning points and the experience achieved about the conduction of Bioavailability/Bioequivalence clinical trials. During the internship I have developed clinical trial assistance activities and I learned a lot about the process of trial conduction, from the submission to the authorities to get their approvals until the process of reporting the results This job was a challenge and a continuous learning process. At the end of this period, I feel it was a rewarded effort and I would like to keep developing my skills in this area.
Ensaios clínicos de Biodisponibilidade/Bioequivalência são uma área promissora em I&D Farmacêutico, e é muito interessante estar envolvida neste âmbito. Durante o estágio pratiquei atividades de assistência a ensaios clínicos de Biodisponibilidade/Bioequivalência sendo este o meu alvo de intervenção na Blueclinical durante dez meses. Durante este tempo também tive oportunidade de exercer atividades de enfermagem de investigação devido à minha formação anterior na área. Este relatório tem como objetivo descrever as atividades em que estive envolvida, os pontos de aprendizagem e a experiência adquirida em relação à condução de ensaios clínicos de Biodisponibilidade/Bioequivalência. Durante o estágio desenvolvi atividades de assistência de ensaios clínicos e aprendi muito sobre o processo de condução do ensaio, desde a submissão do ensaio junto das autoridades para obter a sua autorização até ao processo de relatar os resultados. Este trabalho foi um desafio e um processo de aprendizagem contínua. No final desta etapa, sinto que foi um esforço recompensado e desejo continuar a desenvolver as minhas capacidades nesta área.
Silva, Pedro Miguel Couto Moreira e. "Curricular trainig report as study coordinator in Blueclinical Ltd." Master's thesis, Universidade de Aveiro, 2014. http://hdl.handle.net/10773/15798.
Full textThe present report describes in detail the activities and knowledge aquired during my internship as study coordinator in Blueclinical – Investigação e Desenvolvimento em Saúde, Ltd., in order to obtain the master degree in Pharmaceutical Biomedicine. According to the type of services provided, Blueclinical is formed by three business units: Blueclinical Clinical Research Partnership, Blueclinical Phase I and Blueclinical Research and Development. The fact of belonging to such a company gave me the opportunity to be in touch with different areas of pharmaceutical development and to contact with different research teams, which for me was an added advantage to the integration and consolidation of knowledge, as well as in the development and improvement of soft and hard skills. The main activity developed was the coordination of clinical studies, in Unidade Local de Saúde de Matosinhos, E.P.E., which was one of the institutions that established a partnership with Blueclinical, Ltd. During my internship I was able to contact with various stages of development and coordination of clinical trials, which will be reported in this report.
O presente relatório descreve com detalhe as atividades e aprendizagens adquiridas no âmbito do meu estágio curricular como coordenador de estudos na Blueclinical, Lda., para obtenção do grau de mestre de Biomedicina Farmacêutica. De acordo com o tipo de serviços prestados, a Blueclinical pode ser dividida em três unidades de negócio: Blueclinical Clinical Research Partnership, Blueclinical Phase I e Blueclinical Research and Development. O facto de pertencer a esta companhia deu-me a oportunidade de estar em contacto com diferentes áreas do desenvolvimento farmacêutico e de contactar com diferentes equipas de investigação, o que para mim foi uma vantagem para a integração e consolidação de conhecimento, bem como para o desenvolvimento de hard e soft skills. A principal atividade desenvolvida foi a coordenação de estudos clínicos, na Unidade Local de Saúde de Matosinhos, E.P.E., que se insere na rede de hospitais que estabeleceram parceria com a Blueclinical, Lda. Durante o meu estágio pode contactar com diversas fases de coordenação e desenvolvimento de ensaios clínicos, que serão relatadas nesta dissertação.
Nguyen, Hoang Minh Dung. "Information Extraction from Radiology Reports for a Population Based Cancer Registry." Thesis, The University of Sydney, 2013. http://hdl.handle.net/2123/9466.
Full textOliveira, Joana Pereira. "Curricular training report: clinical studies coordination in a clinical research organization vs an investigational site perspective." Master's thesis, Universidade de Aveiro, 2015. http://hdl.handle.net/10773/15780.
Full textThis report describes my experience of nine months as a trainee of a CRO (Eurotrials, Scientific Consultants), as well as a trainee of a clinical research site (Clinical Academic Center – Braga, Association). This document describes the European framework about clinical research and the Portuguese situation compared to similar countries. The activities developed during this internship are also described. These activities are divided in two phases. The first one occurred in Eurotrials, Scientific Consultants, a CRO specialized in clinical research and scientific advice. The first weeks were dedicated to intensive self-training needed to perform CTA tasks. These tasks included qualification, initiation and monitoring activities related to clinical trials, as well as the development of a quality management system. The second phase took place on 2CA-Braga, a clinical research center located in Hospital of Braga. Clinical studies coordination was the main focus of this second phase of my internship, as well as negotiation of clinical studies agreements. I had also the opportunity to participate in “1as Jornadas de Investigação Clínica e Inovação” (1st Clinical Investigation and Innovation Conference) organized by 2CA-Braga. Globally, this internship was a great opportunity to get knowledge and experience in the implementation and management of clinical trials, in a CRO and clinical research site perspectives. These two perspectives provided an interesting overview about the scientific needs of different players involved in clinical research. To conclude, this internship strengthened the knowledge acquired from my academic background, which make me able to face and overcome new challenges in the clinical research area.
Este relatório descreve a minha experiência de nove meses enquanto estagiária numa CRO (Eurotrials, Consultores Científicos) e num centro de investigação clínica (Centro Clínico Académico – Braga, Associação). Este documento começa por analisar o enquadramento europeu da investigação clínica e, posteriormente, a situação portuguesa comparativamente a países similares. De seguida, são descritas as atividades desenvolvidas no âmbito deste estágio, as quais foram divididas em duas fases. A primeira fase desenrolou-se na Eurotrials, Consultores Científicos, uma CRO especializada em investigação clínica e consultoria científica. As primeiras semanas foram dedicadas ao treino e à formação necessários para o desempenho de tarefas como assistente de estudos clínicos. Estas tarefas incluíram a participação em várias atividades de qualificação, iniciação e monitorização de estudos clínicos, assim como o desenvolvimento e aperfeiçoamento de um sistema de gestão de qualidade. A segunda vertente decorreu no 2CA-Braga, um centro de investigação clínica localizado no Hospital de Braga. Nesta fase, o estágio focou-se essencialmente na coordenação de estudos clínicos, assim como, em atividades relacionadas com o processo de revisão/negociação de contratos financeiros. Para além disso, tive a oportunidade de participar nas “1as Jornadas de Investigação Clínica e Inovação” organizadas pelo 2CA-Braga. Globalmente, o estágio traduziu-se numa excelente oportunidade para ganhar conhecimentos e experiência nas tarefas associadas a projetos e serviços no âmbito da implementação e gestão de estudos clínicos, na perspetiva de uma CRO e de um centro de investigação clínica. A integração destas duas perspetivas permitiu-me identificar e confluir necessidades específicas de diferentes players envolvidos na investigação clínica. Concluindo, este estágio permitiu-me aplicar e aperfeiçoar os conhecimentos adquiridos durante a minha formação académica tornando-me capaz de enfrentar e transpor novos desafios na área da investigação clínica.
Haidamus, Ramzi Albert. "A 68000-based produce sorting microcomputer : graduate clinical research master's report." Scholarly Commons, 1989. https://scholarlycommons.pacific.edu/uop_etds/2172.
Full textCrociati, Naomi. "“L’utilizzo della robotica nella neuroriabilitazione dell’arto superiore: implicazioni cliniche - Case Report"." Bachelor's thesis, Alma Mater Studiorum - Università di Bologna, 2021. http://amslaurea.unibo.it/24582/.
Full textAhmed, Omer Abdelrahim Sidig. "Relationship of TMD diagnosis and self-reported biopsychosocial status of patients attending the TMD clinic." University of the Western Cape, 2018. http://hdl.handle.net/11394/6638.
Full textBackground: This study aimed to investigate a possible relationship between the diagnosis of TMD and biographical, psychological and social status of patients. Materials and Method: All records of patients who attended the TMD clinic in the Mitchells Plain Oral Health Centre in the period from January 2015 to July 2018, and who were examined according to the DC/TMD protocol, were collected. All diagnostic observations, as well as their biographical, psychological and social data were recorded. Statistical analysis was performed by means of comparisons and association analysis among data to evaluate if there were any statistically relevant associations or differences.
Bycroft, Debra. "Probative value of pre-sentence reports for juvenile matters." Thesis, Edith Cowan University, Research Online, Perth, Western Australia, 2020. https://ro.ecu.edu.au/theses/2291.
Full textWilliamson, Jonathan Paul Allan. "Assessing the suitability of cognitive-behavioural therapy for specialised client populations and clinical practice reports." Thesis, University of Birmingham, 2011. http://etheses.bham.ac.uk//id/eprint/3229/.
Full textBustos, Aurelia. "Extraction of medical knowledge from clinical reports and chest x-rays using machine learning techniques." Doctoral thesis, Universidad de Alicante, 2019. http://hdl.handle.net/10045/102193.
Full textFarrica, Anabela de Jesus Prates. "Internship in clinical data management at a clinical research organization." Master's thesis, Universidade de Aveiro, 2015. http://hdl.handle.net/10773/15136.
Full textThe aim of this report is to describe the training activities carried out at the Data Management Sub-Unit of Eurotrials, Scientific Consultants, as part of the 2nd year of the Master’s Program in Pharmaceutical Medicine. This internship was focused on the development of skills and on gaining experience in Clinical Data Management activities. Over the course of this internship, I had the opportunity to build upon the knowledge obtained in the Bachelor’s Degree in Biomedical Sciences and in the Master’s Program in Pharmaceutical Medicine. Concepts, requirements and practices related to Clinical Data Management were explored and strengthened throghout. Furthermore, an unique perspective on the lifecycle of clinical research projects was obtained – that of a CRO. Besides the acquisition of theoretical knowledge, this training period was paramount for the development of a number of social and personal skills that contributed for my profissional growth within the host institution. This document begins by a description of the theoretical principles that set the ground for the Clinical Data Manager’s work. Then, the generic and specific training elements of the curricular training are detailed. After presenting my training activities, I discuss the various challenges I had to overcome during these 9 months. Finally, some personal remarks and conclusions are presented.
Este relatório tem como objetivo descrever as atividades de estágio realizadas na Unidade de Gestão de Dados da Eurotrials, Consultores Científicos, como parte do 2º ano do Mestrado em Biomedicina Farmacêutica. Este estágio focou-se no desenvolvimento de competências e obtenção de experiência em atividades de Gestão de Dados Clínicos. No decurso do estágio tive oportunidade de complementar o conhecimento obtido na Licenciatura em Ciências Biomédicas e no Mestrado em Biomedicina Farmacêutica. Foram aprofundados e explorados os conceitos, requisitos e práticas inerentes à Gestão de Dados Clínicos e obteve-se uma visão única do ciclo de vida de um projeto de investigação clínica – a de uma CRO. Para além da aquisição de conhecimentos teóricos, este período de estágio foi fundamental para o desenvolvimento de um conjunto de aptidões sociais e pessoais que contribuíram para o meu crescimento profissional dentro da instituição de acolhimento. O presente documento começa por expôr os príncipios teóricos que servem de base à atividade do Gestor de Dados Clínicos. Seguidamente, são detalhados os componentes genéricos e específicos de treino adquiridos durante o período de estágio. Depois da apresentação das atividades de estágio, são discutidos os vários desafios enfrentados e é feito um balanço pessoal desta experiência.
Aroney, Christine Margaret. "Patient Reported Outcomes From Clinical Trials in Medical Retina." Thesis, The University of Sydney, 2016. http://hdl.handle.net/2123/16054.
Full textSmith, Anabela Da Silva. "Youth Self-Report : profile patterns of adjudicated adolescents and diagnostic efficiency of clinical scales /." View online ; access limited to URI, 2005. http://0-wwwlib.umi.com.helin.uri.edu/dissertations/dlnow/3206247.
Full textNobre, Ana Rita dos Santos. "Curricular training report about clinical trials monitoring on a CRO full service." Master's thesis, Universidade de Aveiro, 2015. http://hdl.handle.net/10773/13996.
Full textThis report intends to describe the activities carried out under the traineeship which took place in the company Datamédica, Biostatistics Services and Consulting, Inc., a Contract Research Organization (CRO). The internship had the duration of 8 months during which the trainee worked as CRA being the main focus the monitoring of clinical trials. Besides the main activity, have also been developed functions adjacent to the clinical research, such as CTA and Medical Writing areas. This document tries to show the obtained vision and the points of view of the trainee while monitoring clinical trials.
O presente relatório destina-se a descrever as atividades desenvolvidas no âmbito do estágio curricular que teve lugar na empresa Datamédica, Serviços e Consultoria em Bioestatística, Lda., uma Contract Research Organization (CRO). O estágio teve a duração de 8 meses durante os quais a estagiária desempenhou funções de CRA sendo o principal foco a monitorização dos ensaios clínicos. Para além da principal atividade, foram ainda desenvolvidas funções em áreas adjacentes à investigação clínica, tais como CTA e Medical Writing. Este trabalho tenta mostrar a visão obtida e os pontos de vista da estagiária enquanto monitora de ensaios clínicos.
Luz, Guilherme de Sousa. "Curricular internship report in clinical studies monitoring at a full service CRO." Master's thesis, Universidade de Aveiro, 2016. http://hdl.handle.net/10773/16979.
Full textO presente relatório tem como fim descrever as atividades desenvolvidas e experiência e competências adquiridas durante o estágio curricular numa CRO Full Service, a DATAMEDICA – Consultoria e Serviços em Bioestatística, Lda., no âmbito do Mestrado em Biomedicina Farmacêutica. O principal objectivo do estágio foi adquirir conhecimento e competências inerentes ao desempenho do trabalho de Clinical Research Associate. O estágio curricular teve a duração de 8 meses, compreendidos entre setem-bro de 2015 e abril de 2016, tendo o estágio na DATAMEDICA, no entanto, começado em junho de 2015. Este estágio permitiu a realização de várias fun-ções na área da Investigação Clínica, destacando-se a Submissão e Monitori-zação de Estudos Clínicos, Escrita Médica e Gestão de Dados. Neste estágio foi possível aplicar conteúdos teóricos obtidos durante o Mestrado em Biomedicina Farmacêutica e desenvolver competências necessárias, principalmente, à monitorização de ensaios clínicos, mas também às outras atividades supramencionadas. Para além disso, a integração numa equipa multidisciplinar no meio empresarial e interação, aquando fora da empresa, com outros profissionais da área médica e da investigação clínica resultou num crescimento pessoal e profissional. Na secção do estado da arte são abordados temas como a investigação clíni-ca, evolução do ambiente regulamentar a nível global ao longos dos anos. É também feito um panorama dos ensaios clínicos a nível nacional.
The present report aims at describing the developed activities and experiences and skills acquired during the curricular internship at a Full Service CRO, DATAMEDICA – Consultoria e Serviços em Bioestatística, Lda., in the scope of the Pharmaceutical Medicine Master of Science. The main objective of the in-ternship was to acquire knowledge and skills inherent to performing the Clinical Research Associate job. The curricular internship had a duration of 8 months, from September 2015 until April 2016, having the internship at DATAMEDICA, however, started in June 2015. This internship allowed several roles in the Clinical Investigation area to be performed, highlighting the Clinical Studies’ Submission and Moni-toring, Medical Writing and Data Management activities. In this internship it was possible to put into use theoretical concepts obtained during the Pharmaceutical Medicine Master of Science and to develop skills necessary, mainly, to the clinical study monitoring, but also to the other above-mentioned activities. Beyond this, the integration in a multidisciplinary team in a business environment and interaction, when outside the company, with other medical and clinical investigation professionals has resulted in a personal and professional growth. In the state of the art section, clinical investigation and the evolution of the global regulatory environment are mentioned. A panorama of the clinical trials on a national scale is also made.
Vicente, Margarida Isabel de Sousa. "Report of a curricular internship at a full service CRO." Master's thesis, Universidade de Aveiro, 2015. http://hdl.handle.net/10773/14883.
Full textThe present report outlines the activities developed and the acquired experience during the curricular internship at DATAMEDICA, Serviços e Consultoria em Bioestatística, Lda., under the scope of the Pharmaceutical Biomedicine Master Course. The internship, which took place between September 2014 and April 2015, allowed the performance of several activities related to Clinical Research, namely preparation of clinical studies submissions to Competent Authorities; monitoring activities; medical writing and data management. The work developed during this internship was essential both to acquire an important basis regarding new professional, personal and social skills and to develop old ones face to Clinical Research and its most relevant stakeholders, such as communication, concentration, sense of responsibility, organisation and correct response in stressful situations. The internship also allowed me to contact with the daily life activities of a Full Service Clinical Research Organisation (CRO) and put into practice the knowledge acquired at the University.
O presente relatório descreve as atividades desenvolvidas e a experiência adquirida durante o estágio curricular realizado na DATAMEDICA, Serviços e Consultoria em Bioestatística, Lda., no âmbito do Mestrado em Biomedicina Farmacêutica. O estágio, que decorreu de Setembro de 2014 a Abril de 2015, permitiu a realização de diversas atividades relacionadas com Investigação Clínica, das quais se destacam: preparação de submissões de estudos clínicos às Autoridades Competentes; monitorização; medical writing e data management. Todo o trabalho desenvolvido durante este estágio foi fundamental para a aquisição de novas competências e desenvolvimento de antigas, tais como comunicação, concentração, sentido de responsabilidade, organização e resposta em situações de stress, que contribuíram para uma melhor preparação a nível profissional, pessoal e social face à Investigação Clínica e seus principais stakeholders. Adicionalmente, o estágio permitiu contactar com as atividades do quotidiano de uma Clinical Research Organisation (CRO) Full Service e colocar em prática os conhecimentos adquiridos durante a formação na Universidade.
Paul, Lucy Joanne. "An assessment of heart failure screening tools for an outpatient arrhythmia devices clinic." ScholarWorks, 2017. https://scholarworks.waldenu.edu/dissertations/4320.
Full textBrocato, Nicole Whyms. "Information gathered by retrospective, self-report, emotional frequency items in children." Thesis, University of Maryland, Baltimore County, 2014. http://pqdtopen.proquest.com/#viewpdf?dispub=3624332.
Full textRetrospective emotional frequency appraisals are often used in clinical assessment measures, but their suitability for use with children has not been well studied. The aims of this project were to (a) examine whether items that use retrospective frequency structures gather more or less information than items that do not use such structures and (b) examine whether the information gathered by such items differs across children's ages. Method. Data were gathered from 9- to 12-year-old girls who participated in a larger study of a depression treatment protocol. Two sets of five pairs of items were sampled from two children's depression measures. The item pairs contained one item from each measure. One set of item pairs was matched for content and the use of retrospective frequency structures. The other set was matched for content only. Results. For the first research question, information curves for the two item sets were generated using Samejima's (1969) Graded Response Model (GRM). Visual analyses of the information curves provided inconclusive results as to whether the presence of retrospective frequency structures is associated with differences in item information levels. The second research question was conducted in two parts. For both, only data from the 9- and 12-year-old participants were analyzed. In the first part, confirmatory factor analysis was used to analyze measurement invariance across the two groups' responses. Theses analyses showed signs of measurement non-invariance in both item sets. The second part of the analyses was conducted by generating separate GRM information curves for the two age groups and conducting visual analyses of the information curves. These analyses showed that the model which had been used throughout the remainder of the study did not fit the 9-year-old group well. They also showed that the 12-year-old group's information curves varied more in height across measures and item sets than did the 9-year-old group's curves. Discussion. Although the findings failed to shed light on the effects of retrospective frequency structures on children's responding, they highlighted potential differences between the 9- and 12-year-old groups' factor structures and indicated that the 9-year-olds displayed decreased sensitivity to differences in item structure.
Georgievska, Liljana. "Curricular internship report in medical writing at Blueclinical, Portugal." Master's thesis, Universidade de Aveiro, 2015. http://hdl.handle.net/10773/15799.
Full textThe contents of this report are a summary of the activities carried out during the 8-month internship as an Associate Medical Writer at Blueclinical Ltd, Matosinhos, Portugal. Mainly my activities were related to medical writing, particularly writing the clinical research protocols, clinical study reports, writing manuscript and preparing poster presentations. In addition to these activities, I also participated in performance of a clinical trial from beginning to end. During the period of its realization, I was able to familiarize myself with all the steps of the Phase I clinical trial.
O conteúdo deste relatório é um resumo das actividades realizadas durante o estágio de 8 meses, como escritor Médico Associado na Blueclinical, Ltd, em Matosinhos, Portugal. As atividades desenvolvidas foram essencialmente relacionadas com a escrita médica, nomeadamente a escrita dos protocolos de investigação clínica, dos relatórios de ensaios clínicos, redação e preparação de apresentações de pósteres. Além destas atividades, também tive a oportunidade de acompanhar um ensaio clínico de fase I desde o seu início até ao fim. Durante este estudo, foi possível conhecer de perto todas as etapas de realização de ensaios clínicos de fase I.