Relevant bibliographies by topics / Medical regulation

Academic literature on the topic 'Medical regulation'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Contents

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Medical regulation.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Medical regulation"

1

Yam, Carrie H. K., Sian M. Griffiths, S. Liu, Eliza L. Y. Wong, Vincent C. H. Chung, and E. K. Yeoh. "Medical Regulation." Journal of Medical Regulation 102, no. 1 (January 1, 2016): 16–27. http://dx.doi.org/10.30770/2572-1852-102.1.16.

Full text
Abstract:
The licensing and regulation of physicians is an important topic worldwide and is often tied to discussions in various countries of health care system reform. We conducted a review of current practices for regulating physicians as a key group of health care professionals in eight jurisdictions in Asia and other parts of the world in order to draw implications for the development of future regulatory policies in Hong Kong. Jurisdictions studied included Australia, Canada, China, Malaysia, New Zealand, Singapore, the United Kingdom and the United States. A literature search, supplemented by interviews, was conducted. In analyzing information gathered about global regulatory systems, we used a framework for comparing regulatory typology, developed by the RAND Europe research institute. Our review found that the jurisdictions studied exhibited both similarities and differences in terms of how physicians are regulated and by whom. As a result of our search, we were able to identify 10 key trends in international medical regulation of importance to Hong Kong as it considers reforms to its health care system overall:Changes in medical regulation are seen as a way of improving the quality of patient care.Reform of medical regulation often requires government legislation.The creation of common principles for policies, structures and the organization of regulation between professions is an emerging practice.The involvement of lay people on boards and in inquiries is increasingly common.Medical regulation is moving away from models of self-regulation and toward regulatory models that emphasize partnership between professions and the public, physicians and patients.Health care providers and institutional regulators play complementary roles in medical regulation.Regulation impacts the quality of care — not just the detection and remediation of poor performance.Investigatory and disciplinary functions are increasingly separated and organized independently of each other.Continuous Professional Development (CPD) is compulsory for physicians in many jurisdictions.Overseas medical graduates are admitted into practice in different ways from country to country. These trends are important for regulators in all countries to note as they assess the basic structure and effectiveness of their own medical regulatory systems.
APA, Harvard, Vancouver, ISO, and other styles
2

Maak, Travis G., and James D. Wylie. "Medical Device Regulation." Journal of the American Academy of Orthopaedic Surgeons 24, no. 8 (August 2016): 537–43. http://dx.doi.org/10.5435/jaaos-d-15-00403.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Jarow, Jonathan P., and John H. Baxley. "Medical devices: US medical device regulation." Urologic Oncology: Seminars and Original Investigations 33, no. 3 (March 2015): 128–32. http://dx.doi.org/10.1016/j.urolonc.2014.10.004.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Dietrich, Elisabeth M., and Joshua M. Sharfstein. "Improving Medical Device Regulation." JAMA Internal Medicine 174, no. 11 (November 1, 2014): 1779. http://dx.doi.org/10.1001/jamainternmed.2014.3211.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

O'Brien, Claire. "Regulation for medical genetics." Molecular Medicine Today 1, no. 6 (September 1995): 256. http://dx.doi.org/10.1016/s1357-4310(95)90923-0.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Heneghan, Carl, and Mathew Thompson. "Rethinking medical device regulation." Journal of the Royal Society of Medicine 105, no. 5 (May 2012): 186–88. http://dx.doi.org/10.1258/jrsm.2012.12k030.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Galgon, Richard E. "Understanding medical device regulation." Current Opinion in Anaesthesiology 29, no. 6 (December 2016): 703–10. http://dx.doi.org/10.1097/aco.0000000000000391.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Kyselova, O. I., and K. O. Nadtochiy. "Features of legal regulation of labor of medical workers." Legal horizons, no. 24 (2020): 35–40. http://dx.doi.org/10.21272/legalhorizons.2020.i24.p35.

Full text
Abstract:
The work of health care workers is associated with great physical and emotional stress, the need in some cases to work in difficult and life-threatening conditions. This determines some features of the legal regulation of labor relations in this area of activity: additional requirements when concluding an employment contract, preferential working hours and rest time, special rules for part-time work, etc. The specificity of the legal status of medical workers as subjects of labor law is due to both general rules and special regulations on various aspects of their activities. In addition to the general provisions of the Labor Code of Ukraine, the provisions of the law "Fundamentals of the legislation of Ukraine on health care", as well as a number of other regulations apply to medical workers who carry out professional activities. The article describes the regulations governing the employment of health workers, identifies the role of the employment contract in regulating their work, analyzes the features of the legal status of health workers as a subject of labor relations, and identifies a set of problems that arise in health care workers. in the performance of their duties. This topic is of interest not only from a scientific but also from a practical point of view, which necessitates detailed, thorough legal regulation of the work of medical workers and a more careful attitude of the legislator to this area. The urgency of the topic is due to the role of health professionals in the realization of the right of everyone to health care, guaranteed by Art. 49 of the Constitution of Ukraine.
APA, Harvard, Vancouver, ISO, and other styles
9

Nazarenko, G. V. "REGULATION OF COERCIVE MEASURES OF A MEDICAL NATURE." Proceedings of the Southwest State University 21, no. 2 (April 28, 2017): 164–68. http://dx.doi.org/10.21869/2223-1560-2017-21-2-164-168.

Full text
Abstract:
The article is devoted to the legislative regulation of compulsory medical measures. The author shows that the legislative regulations of such measures are not limited to the criminal legislation norms. A number of articles regulating compulsory treatment are envisioned by the Law on Psychiatric Care, as well as other federal regulations. However, the legislative recommendation of coercive measures of medical nature has gaps regarding the implementation of such measures. The article reveals compulsory measures of medical nature, appointed and applied against pedophiles. The author draws attention to the restrictive conditions, the observance of which is necessary for imposition of compulsory treatment for this category of persons. The article emphasizes that the use of coercive measures of medical nature for pedophiles who have committed crimes against the sexual inviolability of minors can continue after serving their sentences if the purposes of applying coercive measures are not met. The basis for the extension of such measures is the public danger of a person suffering from sexual drive disorder. The public danger of persons listed in article 97 of the Criminal Code of the Russian Federation is the only basis for use of coercive measures of medical nature. Persons who are not dangerous are to be treated in medical organizations that provide psychiatric care on a general basis. In necessary, such persons can be send to the handicap centres.
APA, Harvard, Vancouver, ISO, and other styles
10

Powell, Jason L. "Doctoring Medical Governance: Medical Self-Regulation in Transition." Sociology of Health & Illness 33, no. 3 (March 2011): 502–3. http://dx.doi.org/10.1111/j.1467-9566.2011.01336.x.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Medical regulation"

1

Meechan, Kenneth Alastair. "The regulation of British medical practice." Thesis, University of Glasgow, 2002. http://theses.gla.ac.uk/1587/.

Full text
Abstract:
This thesis begins by considering that modern medicine as a profession has tremendous scope for both good and ill, and as an enterprise consumes a vast amount of the national wealth. Against this background, the thesis considers how and why medicine is regulated, and what the effects of this regulation are. The study aims to assess the regulation of the medical profession against the interests of the state, the profession, and the consumers of health care, to see whether the regulatory mechanisms adopted adequately safeguard the interests of all parties concerned with the practice of medicine. The methodology chapter spells out the analytical techniques which the bulk of the thesis utilises and delimits the scope of the research to cover only bodies having a legal genesis and which are universal in application. A series of "core evaluation criteria" are identified against which the four regulatory mechanisms are assessed. Chapters 3 to 6 contain the bulk of the actual research into the four main areas of regulatory endeavour which the study considers; each is analysed in turn in terms of the purpose, mechanism and effect of the regulatory machinery being considered and then assessed against the core evaluation criteria. Finally, the conclusions chapter draws together the different threads which the sector-specific analyses have identified as being points of concern, and the system as a whole is evaluated to see whether the interests of the relevant stakeholders are adequately safeguarded, to identify any regulatory gaps which exist in the present system, and to point out the direction which anyone seeking to improve the system should consider
APA, Harvard, Vancouver, ISO, and other styles
2

Rofougaran, Reza. "DNA precursor biosynthesis-allosteric regulation and medical applications." Doctoral thesis, Umeå : Univ, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-1678.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Stojan, Jure. "Regulation of complementary medical practitioners circa 1920-2000." Thesis, University of Oxford, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.491060.

Full text
Abstract:
$$aThis study describes the changing economic and social role of complementary medicine in twentieth-century Britain; and explains the intensity of its regulation. As a work of economic history, it is guided by three questions: (1) How did industry groups compete among themselves? (2) How did this competition influence the level of regulation which particular groups aspired to? (3) How did these preferences affect the regulatory outcomes?
APA, Harvard, Vancouver, ISO, and other styles
4

Sandvick, Clinton Matthew. "Enforcing Medical Regulation in the United States 1875 to 1915." Thesis, Connect to title online (Scholars' Bank), 2008. http://hdl.handle.net/1794/7783.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Norlin, Nadine. "Disrupted epigenetic regulation causessyndromes of overgrowth- A systematic review." Thesis, Örebro universitet, Institutionen för medicinska vetenskaper, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-66817.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Li, Cathy Shije 1974. "Function and regulation of histone deacetylase 4." Thesis, McGill University, 2006. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=98750.

Full text
Abstract:
Histone acetyltransferases and histone deacetylases (HDACs) maintain dynamic acetylation and deacetylation of histories and other proteins in vivo, and are actively involved in the control of gene transcription and other nuclear processes. One mechanism by which functions of these enzymes are regulated operates through differential intracellular compartmentalization. HDAC4, -5, -7 and -9, the four members of class IIa, shuttle between the nucleus and the cytoplasm in a manner dependent on specific phosphorylation stimulated by several known kinases, and these deacetylases possess intrinsic nuclear import and export signals for dynamic nucleocytoplasmic trafficking. The ability to change their intracellular localization implies that class IIa HDACs have some potential functions in different subcellular compartments. To gain additional insights into this, I first focused on studying the function and regulation of HDAC4. As a result, I identified protein kinase D3 as a novel kinase for HDAC4 and found that this kinase physically interacts with HDAC4 and stimulates its nuclear export. Then I tried to purify protein complexes of RFXANK and ANKRA2, two homologous ankyrin-repeat proteins that are known to associate with HDCA4, using the tandem affinity purification (TAP) strategy. The results that I have obtained reveal a novel mechanism for regulating the nuclear export of HDAC4 and suggest that its cytoplasmic localization may also be indicative of potential cytoplasmic functions rather than just for simple sequestration from its nuclear targets.
APA, Harvard, Vancouver, ISO, and other styles
7

Kazemitabar, Maedeh Assadat. "A multifaceted approach to examining emotion regulation in medical settings." Thesis, McGill University, 2014. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=123282.

Full text
Abstract:
The ability to detect and regulate emotions is an important aspect of emotional intelligence (Mayer, Salovey & Caruso, 2000) that can benefit individuals in their personal well-being and improve social interactions. This thesis examined emotional regulation (ER) in medical students as they participated in an international technology rich learning environment designed to help them learn how best to communicate undesired news to patients (Lajoie et al., 2011). Gross' (1998) process model of ER served as the theoretical model that guided the analysis of regulatory strategies, in a case study (Yin, 2011) of four medical students. An exploratory mixed methods approach was utilised to determine how multichannels of emotion representations (vocal characteristics, motor expressions, attention tendencies) indicate instances of (un)conscious ER. The design of the coding scheme was driven from emotion regulation and coping literature, and methodological techniques were extended from the field of affective computing. Pre-post observations were analyzed to identify patterns of change in using regulatory strategies. Analyses revealed four major findings as evidences of ER: (a) dissociation between emotion channels did occur; (b) changes in emotion expression occurred; (c) unexpected emotions sometimes occurred; and, (d) multiple emotion channels were used to demonstrate emotion regulatory responses. Results also showed that voice modulation (specifically a decrease in voice amplitude) was an important strategy used to extrinsically regulate the patients when giving bad news as it demonstrated an empathetic response by the physician. These findings can provide insights for educators in designing programs to enhance and evaluate ER strategies of students in order to regulate personal emotions as well as the emotional needs of others in stressful situations. This work also makes important contributions to the design of technology-rich environments to embed dynamic ER detection mechanisms that enable systems to gain a more holistic view of the participants, and to adapt instructions based on their affective needs.
La capacité de détecter et de contrôler ses émotions est un aspect important de l'intelligence émotionnelle (Mayer, Salovey & Caruso, 2000) qui peut bénéficier le bien-être des individus et améliorer leurs interactions sociales. Cette thèse a examiné la régulation émotionnelle (RE) chez les étudiants en médecine lors de la participation à un environnement d'apprentissage international riche en technologie visant à les aider à apprendre la meilleure façon de communiquer de mauvaises nouvelles aux patients (Lajoie et al., 2011). Le modèle du processus de RE de Gross (1998) a servi en tant que modèle théorique afin d'analyser les stratégies réglementaires au moyen de l'étude de quatre cas (Yin, 2011). Une approche exploratoire utilisant des méthodes mixtes a été utilisée pour déterminer comment les représentations multidimensionnelles d'émotion se (les caractéristiques vocales, l'incarnation, les tendances d'attention) manifestent chez les cas (in)conscients de RE. Les observations avant et après ont été analysées pour identifier les tendances de changement dans l'utilisation de stratégies de RE. La conception d'un schéma de codage a été tirée de la littérature sur la RE et de l'adaptation, et les techniques méthodologiques ont été étendues du domaine de l'informatique affective. Les analyses ont révélé quatre résultats principaux: (a) la dissociation entre les canaux d'émotion est produite, (b) des changements dans l'émotion ont eu lieu; (c) des émotions inattendues ont eu parfois lieu; et (d) des canaux variées d'émotion ont été utilisés pour démontrer les réponses de RE. Les résultats ont également montré que la modulation de la voix (en particulier la diminution de l'amplitude vocale lors de la sympathie) était une stratégie importante utilisée pour réguler les patients de façon extrinsèque en donnant de mauvaises nouvelles. Ces résultats peuvent guider la conception de programmes visant à améliorer et évaluer les stratégies de RE chez les étudiants afin de réguler les émotions personnelles ainsi que les besoins émotionnels des patients dans les situations stressantes. Ce travail fait également d'importantes contributions à la conception d'environnements riches en technologie visant à intégrer des mécanismes dynamiques de détection de RE qui permettent aux systèmes d'avoir une vue plus globale aux besoins des participants et d'adapter les instructions en fonction de leurs besoins affectifs .
APA, Harvard, Vancouver, ISO, and other styles
8

Higson, Gordon R. "The regulation of medical devices for public health and safety." Thesis, University of Aberdeen, 2000. http://digitool.abdn.ac.uk/R?func=search-advanced-go&find_code1=WSN&request1=AAIU123856.

Full text
Abstract:
Medical products of all kinds have to comply with regulations to satisfy the demand for public health and safety. Medicinal products (drugs) were the first medical products to be regulated in most countries and regulations for medical devices - generally derived from drug regulations - followed. This thesis reviews the development of safety regulation for medical devices from its relatively recent introduction in the 1960s to the present day. The emphasis is on the situation in countries of the European Community but events in these countries are placed in a world-wide context. Landmark events in this process - notably the US Medical Device Amendments of 1976 and the EC Medical Device Directive of 1994 - are analysed and compared. An examination of current regulations in the three major markets for medical devices: Europe, Japan and USA, leads to the identification of quality systems, product standards, effectiveness/performance and post-market controls as key factors in modern regulatory approaches. The emergence of these key factors illustrates the movement towards an engineering, rather than a pharmaceutical, approach to regulation and their place in current and emerging regulations world-wide is discussed. Manufacturers have long pressed for uniformity in national regulations to reduce the time and cost involved in obtaining market approval and their case has been largely accepted by the regulatory authorities. Harmonization in Europe has been achieved as part of the Single Market programme. The last decade has seen remarkable progress towards the further harmonizing of national and regional regulations. The outstanding difficulties, notably controversy over the need for "effectiveness" determination and relative roles of clinical and laboratory testing, are discussed and solutions proposed. The prospects for achieving global harmonization are examined and a possible future global system is described.
APA, Harvard, Vancouver, ISO, and other styles
9

Fiandalo, Michael Vincent. "PROTEASOME REGULATION OF CASPASE-8: SIGNIFICANCE IN CANCER." UKnowledge, 2012. http://uknowledge.uky.edu/biochem_etds/3.

Full text
Abstract:
Anti-tumor therapeutic strategies based on combinations of chemotherapeutic agents with a death inducing ligand such as TNF-α Related Apoptosis Inducing Ligand (TRAIL), are directed towards selective and effective cancer cell apoptosis and enhanced therapeutic response. We previously demonstrated that proteasome inhibition sensitizes TRAIL resistant prostate cancer cells to TRAIL-mediated apoptosis via stabilization of the active p18 subunit of initiator caspase-8. The present study investigated the functional link between caspase-8 and the proteasome, by analyzing the impact of caspase-8 ubiquitination and proteasomal degradation on the outcomes of the extrinsic apoptosis pathway in cancer cells. Caspase-8 ubiquitination status was assessed by polyubiquitin immunoprecipitation (IP) and fluorescent microscopy. Apoptosis induction in response to death receptor stimuli or proteasome inhibitor was evaluated using the Annexin V/Propidium iodide staining (PI). To determine the consequences of proteasome inhibition on caspase-8 stability, trafficking, and activity following death receptor activation, we used the TRAIL-resistant human prostate cancer LNCaP cells, and the caspase-8 deficient Neuroblastoma 7 (NB7) cells, as cellular models for reconstituting the non-cleavable mutant forms of caspase-8. Our findings demonstrate that the non-cleavable forms of caspase-8 are capable of inducing apoptosis comparably to wild-type caspase-8 upon treatment with proteasome inhibitor and GST-TRAIL. Furthermore, caspase-8 processing into its active subunits preceded caspase-8 polyubiquitination, implicating caspase-8 processing as a potential regulatory mechanism, rather than a requirement for caspase-8 activation in apoptosis induction. The mechanistic control of caspase-8 by ubiquitination in cancer cells may have significant significance in bypassing mechanisms of therapeutic resistance in human tumors and optimization of anti-cancer treatment strategies in human tumors and optimization of anti-cancer treatment strategies.
APA, Harvard, Vancouver, ISO, and other styles
10

Aziz, Miriam. "The regulation of medical research involving human subjects : a comparative study." Thesis, University of Edinburgh, 1998. http://hdl.handle.net/1842/21357.

Full text
Abstract:
This thesis is concerned with finding an appropriate legal response to medical research involving human subjects. The first section contains Chapter One which consists of an historical account of forms of unethical research and asks two questions; first, how could such things have been done in the name of research? Secondly, how could society allow them to take place? How were the safeguards overridden? What was the environment or climate within which unethical research was allowed to flourish? The history of the regulation of medical research testifies to the social climate within which research has been conducted. This includes the evolution of the doctor as scientist which led to the objectification of human beings as research subjects, the presence of ideologies in times of war, for instance, which took hold of national consciousness and conscience thereby shifting the goal posts of justification, and the development and maturing of medical careers. Chapters Two, Three and Four comprise section two and deal with the intellectualisation of questions of research at the abstract level of the medico/legal debate. In particular, Chapter Two outlines the terminology of medical research, the monopoly over which has been secured by scientists through scientific reasoning. Chapter Three considers legal reasoning in relation to the concept of informed consent and considers the implications of an approach based on medical negligence, in itself a retrospective 'after the fact' approach; it will be argued that medical research should be viewed prospectively within a framework which is more informed by public than private law. Chapter Four considers the role of moral reasoning in relation to its main protagonists, 'bioethicists', who retain a firm grip on the ethical implications of medical research. An alternative rationale will be suggested which is both universally applicable and normatively neutral. It will be further argued that moral reasoning should involve the public sphere and should not be confined to the private realms consisting of the educated intuitions of researchers and other members of the professional elite. The third section consists of Chapters Five and Six and are concerned with the applied level of the medical research debate as seen in research ethics committees in both the United Kingdom and Germany.
APA, Harvard, Vancouver, ISO, and other styles
More sources

Books on the topic "Medical regulation"

1

Heller, Mark A. Guide to medical device regulation. Washington, D.C: Thompson Pub. Group, 1993.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
2

Heller, Mark A. Guide to medical device regulation. Washington, DC: Thompson Pub. Group, 1997.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
3

Chamberlain, John Martyn. The Sociology of Medical Regulation. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-4896-5.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

FDA regulation of medical devices. Buffalo Grove, IL: Interpharm Press, 1995.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
5

Medical device design and regulation. Milwaukee, Wis: ASQ Quality Press, 2011.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
6

Chamberlain, John M. Doctoring medical governance: Medical self-regulation in transition. Hauppauge NY: Nova Science Publishers, 2009.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
7

Chamberlain, John M. Doctoring medical governance: Medical self-regulation in transition. New York: Nova Science Publishers, 2009.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
8

Davies, Mark. Medical self-regulation: Crisis and change. Aldershot, Hants, England: Ashgate, 2007.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
9

Michael, Moran. States, regulation, and the medical profession. Buckingham: Open University Press, 1993.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
10

American Bar Association. Section of Science & Technology Law, ed. Medical biotechnology: Premarket and postmarket regulation. Chicago, Illinois: American Bar Association, Section of Science & Technology Law, 2015.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Book chapters on the topic "Medical regulation"

1

Manz, Dan. "Legislation, regulation, and ordinance." In Emergency Medical Services, 36–43. Chichester, UK: John Wiley & Sons, Ltd, 2015. http://dx.doi.org/10.1002/9781118990810.ch78.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Al-Bar, Mohammed Ali, and Hassan Chamsi-Pasha. "Regulation of Medical Profession and Medical Research." In Contemporary Bioethics, 85–103. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-18428-9_5.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Ochs, Raymond S. "Medical Issues Related to Metabolism." In Metabolic Structure and Regulation, 241–54. Boca Raton : CRC Press, 2018.: CRC Press, 2017. http://dx.doi.org/10.1201/9781315373133-10.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Szépfalusi, Zsolt, and Thomas Eiwegger. "Genetic Regulation of IgE." In Encyclopedia of Medical Immunology, 335–39. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4614-9194-1_81.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Liebenau, Jonathan. "Science-based Industry: Scientific Disputes and Government Regulation." In Medical Science and Medical Industry, 79–97. London: Palgrave Macmillan UK, 1987. http://dx.doi.org/10.1007/978-1-349-08739-6_6.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Wiersinga, Joris. "Regulation of Medical Digital Technologies." In Human–Computer Interaction Series, 277–95. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-60672-9_13.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Mason, Shuna. "European Regulation of Medical Devices." In The Textbook of Pharmaceutical Medicine, 418–34. Oxford, UK: Blackwell Publishing Ltd., 2013. http://dx.doi.org/10.1002/9781118532331.ch21.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Birmingham, Daniel J. "Complement Regulation in the Kidney." In Encyclopedia of Medical Immunology, 303–7. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-0-387-84828-0_57.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Mcbride, W. J., J. M. Murphy, L. Lumeng, and T. K. Li. "Serotonin Regulation of Alcohol Drinking." In Medical Science Symposia Series, 375–81. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1920-7_44.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Chowdhury, Nupur. "Conceptualizing Multilevel Regulation." In European Regulation of Medical Devices and Pharmaceuticals, 25–46. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-04594-8_2.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Medical regulation"

1

Wang, Na, and Jinguo Wang. "Development and Regulation of Medical Internet." In 2018 8th International Conference on Manufacturing Science and Engineering (ICMSE 2018). Paris, France: Atlantis Press, 2018. http://dx.doi.org/10.2991/icmse-18.2018.14.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Savoshchikova, Evgenia. "Medical Errors Or Harm Resulting From Medical Intervention: Limits Of Legal Regulation." In International Scientific Conference «Social and Cultural Transformations in the Context of Modern Globalism» dedicated to the 80th anniversary of Turkayev Hassan Vakhitovich. European Publisher, 2020. http://dx.doi.org/10.15405/epsbs.2020.10.05.126.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

"GenCoNet: medical information system to support the treatment of co-morbid diseases." In Bioinformatics of Genome Regulation and Structure/ Systems Biology. institute of cytology and genetics siberian branch of the russian academy of science, Novosibirsk State University, 2020. http://dx.doi.org/10.18699/bgrs/sb-2020-271.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

"Named entity recognition in medical texts in Russian using deep learning models." In Bioinformatics of Genome Regulation and Structure/ Systems Biology. institute of cytology and genetics siberian branch of the russian academy of science, Novosibirsk State University, 2020. http://dx.doi.org/10.18699/bgrs/sb-2020-114.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Wang, Dong, Delroy Smith, Ray Krasinski, Monisha Ghosh, and Anuj Batra. "Emerging spectrum regulation for Medical Body Area Network." In 2013 IEEE International Conference on Body Sensor Networks (BSN). IEEE, 2013. http://dx.doi.org/10.1109/bsn.2013.6575476.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Zhang, Gaoyan, Li Yao, and Zhiying Long. "Alteration of functional connectivity during real-time fMRI regulation of PCC." In SPIE Medical Imaging. SPIE, 2012. http://dx.doi.org/10.1117/12.911134.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Sereda, E. V., and O. A. Zalata. "INDIVIDUAL MINUTE AS A REFLECTION OF ADAPTIVE CAPACITY THE DIFFERENT AGE MEDICAL STUDENTS." In MODERN PROBLEMS IN SYSTEMIC REGULATION OF PHYSIOLOGICAL FUNCTIONS. NPG Publishing, 2019. http://dx.doi.org/10.24108/5-2019-confnf-69.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

"Whole genome analysis of clinical Staphylococcus aureus multi-drug resistant isolates from Moscow medical center." In Bioinformatics of Genome Regulation and Structure/ Systems Biology. institute of cytology and genetics siberian branch of the russian academy of science, Novosibirsk State University, 2020. http://dx.doi.org/10.18699/bgrs/sb-2020-040.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Sargunam, B., and S. Anusha. "IoT Based Mobile Medical Application for Smart Insulin Regulation." In 2019 IEEE International Conference on Electrical, Computer and Communication Technologies (ICECCT). IEEE, 2019. http://dx.doi.org/10.1109/icecct.2019.8869227.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Gao, Ling, Yutian Lin, Huibin Lin, Xiaoyi Jia, Jianqun Lin, and Jianqiang Lin. "Mathematical modeling of lac operon regulation dynamics." In International conference on Human Health and Medical Engineering. Southampton, UK: WIT Press, 2014. http://dx.doi.org/10.2495/hhme130611.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Reports on the topic "Medical regulation"

1

Cicala, Steve, Ethan M. J. Lieber, and Victoria Marone. Cost of Service Regulation in U.S. Health Care: Minimum Medical Loss Ratios. Cambridge, MA: National Bureau of Economic Research, April 2017. http://dx.doi.org/10.3386/w23353.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Allen, Robin, and Paul Gertler. Regulation and the Provision of Quality to Heterogenous Consumers: The Case of Prospective Pricing of Medical Services. Cambridge, MA: National Bureau of Economic Research, May 1987. http://dx.doi.org/10.3386/w2269.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Brahmavar, Suresh M., Fred Hetzel, Patrick Clark, Penny J. Smalley, Cathy Miller, Robert Watkins, Leslie Pollard, Vangie Paschall-Dennis, and Terry LaFrance. Medical Lasers: Quality Control, Safety Standards, and Regulations. AAPM, 2001. http://dx.doi.org/10.37206/72.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Einav, Liran, Amy Finkelstein, Yunan Ji, and Neale Mahoney. Voluntary Regulation: Evidence from Medicare Payment Reform. Cambridge, MA: National Bureau of Economic Research, May 2020. http://dx.doi.org/10.3386/w27223.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Wiley, Jenny L., Camille K. Gourdet, and Brian F. Thomas. Cannabidiol: Science, Marketing, and Legal Perspectives. RTI Press, April 2020. http://dx.doi.org/10.3768/rtipress.2020.op.0065.2004.

Full text
Abstract:
Recent loosening of legal restrictions on cannabis and its chemical constituents, including phytocannabinoids such as Δ9-tetrahydrocannabinol (THC) and cannabidiol (CBD), has led to rapid proliferation and wide availability of products containing CBD. Although using pure CBD does not result in THC-like intoxication, it is not risk-free. In this review, we examine CBD from scientific, marketing, and regulatory perspectives. Specifically, we evaluate the evidence used to support statements concerning CBD’s real and putative medical effects and discuss misleading information that has been used in marketing approaches. Also, we explore the current legal landscape surrounding CBD. We conclude that further research is necessary to clarify legitimate therapeutic effects of CBD. Federal regulation is also necessary to assure quality, safety, and efficacy of CBD products. Until new regulations are enacted to ensure purity and label accuracy, consumers should balance any perceived benefits of CBD use against potential risks associated with using products of unknown quality.
APA, Harvard, Vancouver, ISO, and other styles
6

DEPARTMENT OF THE ARMY WASHINGTON DC. Medical Administration: Patient Regulating To and Within the Continental United States. Fort Belvoir, VA: Defense Technical Information Center, March 1990. http://dx.doi.org/10.21236/ada403552.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Finkelstein, Amy. Minimum Standards and Insurance Regulation: Evidence from the Medigap Market. Cambridge, MA: National Bureau of Economic Research, May 2002. http://dx.doi.org/10.3386/w8917.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Grennan, Matthew, and Robert Town. Regulating Innovation with Uncertain Quality: Information, Risk, and Access in Medical Devices. Cambridge, MA: National Bureau of Economic Research, February 2015. http://dx.doi.org/10.3386/w20981.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Jones, E. D., W. W. Banks, T. J. Altenbach, and L. E. Fischer. Relative risk analysis in regulating the use of radiation-emitting medical devices. A preliminary application. Office of Scientific and Technical Information (OSTI), September 1995. http://dx.doi.org/10.2172/105843.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Polyakova, Maria. Regulation of Insurance with Adverse Selection and Switching Costs: Evidence from Medicare Part D. Cambridge, MA: National Bureau of Economic Research, September 2015. http://dx.doi.org/10.3386/w21541.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Medical regulation' for particular source types:
Journal articles Dissertations / Theses Books
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography