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Articles de revues sur le sujet "Product safety – Law and legislation – European Union countries"
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Klovach, E. V., G. M. Seleznev et A. Yu Sulimov. « Relationship between the Classification of Chemical Products and Criteria for Qualifying Objects as Hazardous Production Facilities ». Occupational Safety in Industry, no 10 (octobre 2022) : 27–32. http://dx.doi.org/10.24000/0409-2961-2022-10-27-32.
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In 2002 the international community adopted a new system of hazard classification and labeling of chemical products, which is recommended to be implemented by all the Member- countries of the United Nations through national legislation and international acts. Within the frame of the implementation of this decision, in 2015 the amendments were made to the Directive of the European Community of June 24, 1982, № 82/501/EEC on the prevention of major industrial accidents, and to the United Nations Convention onthe prevention of major industrial accidents, and a little later to the national legislation of the European countries establishing measures on preventing major accidents. In 2017, the countries of the Eurasian Economic Union adopted the technical regulation on the safety of chemical products, which establishes classification criteria that are completely identical to the criteria for the system of hazard classification and labeling of chemical products. Entry into force of the technical regulation of the Eurasian Economic Union will lead to the need for amending all theregulatory legal acts and regulations that contain regulations based on the classification of chemical products, including in the Federal Law № 116-FZ of July 21, 1997, On industrial safety of hazardous production facilities. The task of harmonizing the legislation on industrial safety with the international documents in terms of the classification of chemicals was planned to be solved when developing a new law on industrial safety. During the discussion, the developers encountered different approaches to the definition of classes of hazardous substances, the analysis of which became the subject of this article. The authors formulated proposals that can be used at the next round of harmonization of the Russian legislation on industrial safety with the international documents. When preparing proposals with classes and lists of hazardous chemicals for use in the industrial safety legislation, a comparison was made not only of the definitions of classes of chemicals in different documents, but also of their quantities, which are the criteria for qualifying objects as hazardous production facilities. It is noted that the term «flammable liquids», used in 116-FZ, practically does not occur in the international classifications, therefore, when developing new documents, it was proposed not to use it.
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Zajc, Katarina, et Breda Mulec. « New Challenges in the Filed of Ambient Air Protection with the Emphasis on Economic (in)efficiencies of Chimney Sweeping Services ». Lex localis - Journal of Local Self-Government 11, no 3 (1 juillet 2013) : 311–24. http://dx.doi.org/10.4335/11.2.311-324(2013).
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This paper analyzes new challenges in the field of ambient air protection, such as the use of new energy-generating products, and assesses the air quality protection responsibilities of local communities in European Union (EU) Member States. Domestic heating systems are a major source of air pollution. Thus, chimney-sweeping services are very important and must be regulated to provide fire safety and guarantee better ambient air quality. This paper analyzes Slovenian legislation regulating chimney-sweeping services and compares the Slovenian laws with comparable laws of other European countries and the national laws of EU Member States to examine the laws’ effectiveness in regulating and protecting air quality. More specifically, the paper uses legal and economic analyses to examine the efficiency of current legislation pertaining to chimney-sweeping services. The paper concludes that, consistent with theories of asymmetric information and negative externalities, licensing would be more effective in meeting the challenges of ambient air protection than current exclusive concession agreements, which effectively establish geographical monopolies in chimney-sweeping services.
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Dukhnevych, Andrii V., Nataliia V. Karpinska et Iryna V. Novosad. « Phytosanitary examination : Ukraine experience and international standards ». Journal of the National Academy of Legal Sciences of Ukraine 28, no 2 (25 juin 2021) : 262–68. http://dx.doi.org/10.37635/jnalsu.28(2).2021.262-268.
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The article explores Ukraine’s experience in conducting phytosanitary expertise based on international standards. It was stated that Ukraine should develop a series of draft in national legislation in the field of quarantine and plant protection, which would be adapted to the legislation of the European Union and at the same time meet the requirements of the International Plant Protection Convention. In this area, Ukraine has already partially implemented some structural reforms in the phytosanitary sector, but these processes require continued state support and encouragement, international coordination that will facilitate the development of agriculture in general. Such coordination can be undertaken primarily in the framework of international universal organisations within the UN system, in particular within FAO. It has been emphasised that Law of Ukraine No. 2501-VIII “On Amendments to Certain Legislative Acts of Ukraine on Regulation of Some Phytosanitary Procedures” came into force on February 2, 2019. Among the innovations are the granting of the right to carry out expert examination to private laboratories, new terms in the field of plant quarantine and the creation of the Register of Phytosanitary Certificates issued. It has been concluded that Ukraine is currently actively applying international standards, participating in their development and registering official translations of international standards for phytosanitary measures. Developing national and applying international standards, as a key factor in creating a quality system in the field of plant quarantine, not only ensure full fulfilment by Ukraine of its obligations under the IPPC and SPS, agreeing on the phytosanitary safety of exported quarantine cargoes, but also increase the competitiveness of the domestic vegetal products in the world market. This creates a positive image of Ukraine as a reliable trading partner that does not violate the requirements of other countries and guarantees the conformity of product quality, phytosanitary procedures to internationally recognised standards. Therefore, for qualified phytosanitary examinations, the mechanism of guaranteeing compliance with national and international standards, amending legislation, introducing effective penalties for violation of the rules and procedure for conducting phytosanitary examinations should be a promising area
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Kiseļova, Olga, Baiba Mauriņa, Venta Šidlovska et Jānis Zvejnieks. « The Extent of Extemporaneous Preparation and Regulatory Framework of Extemporaneous Compounding in Latvia ». Medicina 55, no 9 (26 août 2019) : 531. http://dx.doi.org/10.3390/medicina55090531.
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Background and objectives: Extemporaneous preparations are pharmaceutical preparations individually prepared for a specific patient or patient group, but also high-risk products accompanied by doubts regarding their safety and quality. Legislation regulating the compounding of extemporaneous preparations is not harmonized among European countries. This problem is partially resolved by Resolution CM/Res(2016)1 on quality and safety assurance requirements for medicinal products prepared in pharmacies for the special needs of patients. In order to understand the relevance of extemporaneous compounding in Latvia and the fulfillment of the abovementioned resolution’s requirements, it is essential to get information about the volume and breakdown of sales of extemporaneous medicinal products in community pharmacies. The purpose of this survey is to identify the sales volume of extemporaneous preparations in community pharmacies in Latvia in 2017 by analyzing unpublished data of the State Agency of Medicines (SAM), as well as comparing Latvian laws with the requirements of the resolution. Materials and Methods: A separate Microsoft Excel spreadsheet was prepared for each statistical region in order to summarize the unpublished information of SAM on the turnover of extemporaneous preparations in 2017 in all Latvian statistical regions. In order to compare the regulatory framework in Latvia with the resolution, the Latvian Pharmaceutical Law and the Cabinet of Ministers Regulations regulating prescription, compounding and control of extemporaneous preparations in community pharmacies were analyzed. Results: Only 280 of 384 pharmacies submitted a report of sales of extemporaneous preparations for 2017 to the SAM. These pharmacies represented all Latvian statistical regions. Extemporaneous preparations were mostly sold in Riga (78.93%). The Latvian regulation does not include all paragraphs of the resolution. Most of the paragraphs of the resolution are described in Latvian regulatory enactments only partially. Conclusions: The total number of compounding pharmacies evidence that the service is needed. Latvian example highlights a necessity for European Union countries to compare their national legislation with the requirements of the resolution’s last version and, if necessary, implement relevant amendments.
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Rіeznikov, Valeriі. « State industrial policy in conditions European integration of Ukraine ». Public administration and local government 45, no 2 (23 juillet 2020) : 146–53. http://dx.doi.org/10.33287/102030.
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Since the beginning of 2020, there have been crisis phenomena around the world due to the global slowdown in economic growth and the introduction of quarantine due to the coronavirus pandemic. In this situation, the most vulnerable are developing countries with a small margin of safety, which, unfortunately, also applies to Ukraine, whose economy is open and highly dependent on external markets.
Due to the slowdown in the growth of the global economy, the situation in one of the main export industries of Ukraine – industry is deteriorating first of all. The European Union has become one of the important export markets for Ukraine’s industrial products in recent years, which has raised the issue of shaping a relevant state industrial policy in today’s challenging environment. The purpose of the article is to determine the directions of formation and implementation of state industrial policy in the conditions of European integration of Ukraine in modern conditions. In 2020, due to the economic crisis and the pandemic of the coronavirus, the Ukrainian industry may lose even more due to low demand for ferrous metals in world markets, including in EU countries.
The Agreement on Conformity Assessment and Acceptance of Industrial Products is a way of eliminating technical barriers to trade between Ukraine and the EU. The Agreement on Conformity Assessment and Acceptance of Industrial Products is a type of mutual recognition agreement that requires a partner country to align its legislation, practices and infrastructure with EU rules.It is envisaged that in the sectors covered by this Agreement, Ukrainian exporters will be able to label their products with the CE mark and to sell them freely on the EU market without additional EU certification. Potentially, the Agreement on Conformity Assessment and Acceptance of Industrial Products could cover up to a fifth of Ukraine’s exports to the EU, notably mechanical engineering products. The formation and implementation of state industrial policy in the conditions of European integration of Ukraine should take place using the following algorithm:1. Study of the new EU Regulation 2019/1020 of 20.06.2019 on market surveillance and conformity of products and elaboration of relevant amendments to the legislation of Ukraine.2. Concentration of the function of legal coordination of draft regulatory acts (including technical regulations) aimed at implementing the Association Agreement and preparation for the Agreement on Conformity Assessment and Acceptance of Industrial Products in one state instance, equipped with specialized personnel with adequate knowledge of EU law and languages.3. Strengthening the requirements for the accreditation and oversight process for accredited bodies, as well as the process of designating and monitoring conformity assessment bodies to ensure that their technical competence is adequate and to prevent fraud and the use of fraudulent practices.4. In the absence of a rapid prospect of concluding an Agreement on Conformity Assessment and Acceptance of Industrial Products, the harmonization of procedures and requirements that are too burdensome for exporters and importers, first and foremost.5. Paying particular attention to capacity building of state market surveillance authorities.6. Raising awareness of business entities and enhancing the role of business associations in raising such awareness.7. Increasing the EU’s interest in providing Ukraine with effective technical assistance for the development of legislation and the proper functioning of quality infrastructure and market surveillance authorities.
Introduce the position of Deputy Prime Minister for Industry and launch support programs for the real economy.
Thus, Ukraine’s further integration with the European Union is largely linked to the formulation and implementation of relevant industrial policy, which should be to continue reforming all sectors of the economy, in particular, to modernize the industrial complex. And the signing of the Agreement on Conformity Assessment and Acceptance of Industrial Products in the three priority sectors («industrial visa waiver») in the medium term should become one of the main foreign economic priorities of Ukraine’s European integration in the face of the current challenges of today.
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Khitska, O., et R. Gerard. « INTERNATIONAL AND NATIONAL LEGISLATION TO CONTROL MICTOXINS IN FOOD : REVIEW ». Naukovij vìsnik veterinarnoï medicini, no 1(149) (30 mai 2019) : 30–40. http://dx.doi.org/10.33245/2310-4902-2019-149-1-30-40.
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Today, the problem of monitoring mycotoxins has become global in connection with climate change, a violation of the ecological balance for the use of intensive technologies for processing crops, through air pollution and the accumulation of products of photochemical reactions (photooxidants), which leads to a decrease in plant resistance to phytopathogens. Every year, the problem of mycotoxicosis is exacerbated, as toxic fungi adapt quickly to new technologies and modern plant protection products. The increase in mycotoxins in foods also relates to the widespread use of nitrogen fertilizers and pesticides. Natural toxins create risks for the health of humans and animals, affect food security and nutrition, reducing people's access to healthy food. The World Health Organization is constantly appealing to national authorities to monitor and ensure that the levels of the most relevant natural toxins in foods are as low as possible and consistent with both national and international requirements. Ukraine's membership in the WTO, an association with the European Union, and the expansion of international trade require solutions to the issues of free movement of goods, safe and healthy food, and, accordingly, an adequate level of protection of life and health of people. One of the most important ways to solve them is to improve and harmonize national food legislation in line with international standards, including on the control of mycotoxins. The purpose of our work was to conduct an analysis of literary sources, international and national legislative acts on the control of mycotoxins in food products throughout the food chain. To prepare the publication, we have used literary sources on the subject of publication, as well as we have conducted a comparative analysis of national and international legislative acts regulating procedures and methods for controlling the residues of mycotoxins in food. An analysis of numerous sources has shown that the issue of monitoring mycotoxins in foods, improving laboratory control and risk-based approach to preventing foodborne mycotoxicosis worries scientists from different countries, including Ukrainian. The analysis of national legislation shows that national standards on maximum levels of pollutants have been revised in Ukraine and a number of standards have been harmonized for methods of monitoring the residues of mycotoxins in feed for productive animals, food products of animal and vegetable origin. Key words: mycotoxins, food chain, food, international law, national legislation, control, safety, risks.
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Oelze, Ilse-Barbara, Kurt Neeser et Elvira Müller. « PP31 Medical Device Regulation : What Is New ? » International Journal of Technology Assessment in Health Care 35, S1 (2019) : 42–43. http://dx.doi.org/10.1017/s0266462319001958.
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IntroductionIn 2017, the European Union (EU) commission released the final versions of the Medical Device Regulation (MDR) and In-vitro Diagnostic Device Regulation. These regulations will replace the EU directives (Medical Device Directive [MDD], In-vitro Diagnostic Device [IVDD], and Active Implantable Medical Device [AIMD]). EU regulations are effective in all EU countries at date of publication. In contrast, the EU directives must be implemented in national law first.MethodsGuidelines and respective legislation, consultation results and methods/medical device (MD) evaluations were reviewed and analyzed. Decision criteria and reasoning, assessment outcomes and potential impact on price negotiations were the main aspects for comparison.ResultsManufacturers have to be aware of the importance of clinical data for demonstrating the compliance of their products. This applies both to the approval of the products and the “post-market activities” and particularly to the “post-market clinical follow-up” for which requirements for Class I and II products need to be further developed. The MDR requires manufacturers to collect clinical data before and after approval, which could lead to excessive documentation requirements. The term “sufficient clinical data” from the MDR is unclear. A functional Eudamed specification is necessary, which enables an automated processing of relevant data. A stronger involvement in the evaluation process is needed as well as more transparency in the Joint Federal Committee (G-BA) and faster evaluation processes.ConclusionsThe MDR increases the burden especially for small businesses, and it is doubtable that the ultimate goal – improving patient safety – will be achieved. The increased demands and rising costs of the new EU MDR and bottlenecks at Notified Bodies can be a risk for the MD industry. Due to the general reduction in the remuneration for services with a high proportion of technical services, it is feared that products will be withdrawn from the market for economic reasons or that they will not be marketed.
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Lähteenmäki-Uutela, Anu, Moona Rahikainen, María Teresa Camarena-Gómez, Jonna Piiparinen, Kristian Spilling et Baoru Yang. « European Union legislation on macroalgae products ». Aquaculture International 29, no 2 (20 janvier 2021) : 487–509. http://dx.doi.org/10.1007/s10499-020-00633-x.
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AbstractMacroalgae-based products are increasing in demand also in Europe. In the European Union, each category of macroalgae-based products is regulated separately. We discuss EU legislation, including the law on medicinal products, foods including food supplements and food additives, feed and feed additives, cosmetics, packaging materials, fertilizers and biostimulants, as well as biofuels. Product safety and consumer protection are the priorities with any new products. Macroalgae products can be sold as traditional herbal medicines. The novel food regulation applies to macroalgae foods that have not previously been used as food, and organic macroalgae are a specific regulatory category. The maximum levels of heavy metals may be a barrier for macroalgae foods, feeds, and fertilizers. Getting health claims approved for foods based on macroalgae is demanding. In addition to the rules on products, the macroalgae business is strongly impacted by the elements of the general regulatory environment such as agricultural/aquacultural subsidies, maritime spatial planning and aquaculture licensing, public procurement criteria, tax schemes, and trade agreements.
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Čapla, Jozef, Peter Zajác, Katarína Ševcová, Jozef Čurlej et Martina Fikselová. « Overview of the milk and dairy products legislation in the European Union ». Legestic 1 (5 janvier 2023) : 1–16. http://dx.doi.org/10.5219/legestic.1.
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European Union legislation laying down rules for the dairy sector. The legislation defines the conditions under which milk and milk products intended for human consumption can be imported into the EU. Milk and milk products must come only from third countries that appear on the list of authorized countries. Establishments, where milk and milk products are produced, must be approved for export. The TRACES system is used on imports and the consignment must be accompanied by a certificate. This system ensures product traceability and prevents the introduction of diseases. An important role is delegated to the designated border control posts (BCPs) where the appropriate customs and veterinary inspections are performed by government institutions of the country. The European Union has adopted legislation to ensure the safety of food placed on the market in EU member countries. This legislation sets general hygienic requirements for food production based on the good manufacturing practice and the HACCP system. The criteria for microorganisms, chemicals, and applicable food additives are set. Also, the legislation contains requirements for product labeling. Part of the legislation concerns the common organization of the market in milk and milk products. These regulations contain rules for direct payments, subsidies, define the school milk system, etc. Specific legislation creates rules for organic bio food production, for production and labeling of products with the Protected Geographical Indication, Protected Designation of Origin, and Traditional Specialty Guaranteed. There is also legislation that defines the labeling of products intended for specific populations, e.g. gluten-free foods, lactose-free foods, etc. Areas not regulated by the legislation include the labeling of products with certification marks designed to highlight the suitability of food for religious purposes or quality certification.
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Kravchuk, Natalia. « REGULATION OF GENETICALLY MODIFIED ORGANISMS IN EUROPEAN UNION : THE NECESSITY TO UPDATE THE LEGISLATION IS OBVIOUS ». Pravovedenie IAZH, no 4 (2022) : 83–95. http://dx.doi.org/10.31249/rgpravo/2022.04.07.
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The review is devoted to the problems of legislative regulation of genetically modified organisms in European Union. EU legislation in this field is more strict than that in the other countries. It is based on the difference between natural organisms and those created artificially through genetic engineering. The core of the GMO legislation is the precautionary principle which aims at protecting environment and human health. This principle is not compatible with the principle of presumed safety of the product which underpins legislation of many countries-EU trade partners. Asymmetry in regulation leads to complications in trade and to noncompliance with EU legislation. A control of GMO non-authorized for use on the territory of EU in imported food and feed is realized through inspections, conducted on the level of EU states. Undertaken measures, however, can not guarantee consumer’s freedom of choice. All the mentioned problems in the field of GMO regulation dictate the necessity to update the relevant legislation.
Thèses sur le sujet "Product safety – Law and legislation – European Union countries"
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Thebaud, Edern. « Les produits-frontière dans la législation alimentaire de l'Union européenne : émergence d'une santé alimentaire entre logique du marché intérieur et exigences de sécurité ». Doctoral thesis, Universite Libre de Bruxelles, 2012. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/209577.
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Si le droit connaît les médicaments et les denrées alimentaires, il ne reconnaît pas les alicaments. Or, ces dernières années ont vu l’apparition et le développement, sur le marché de l’Union européenne, de « produits-frontière » c'est-à-dire de produits se trouvant à la frontière entre les médicaments et les aliments. Confrontées à un vaste conflit de qualification causé par l’ambivalence conceptuelle des « produits-frontière », les institutions de l’Union ont, au nom de la libre circulation des marchandises ainsi que de la nécessité d’une protection accrue des consommateurs et de la santé publique, entamé, dès le début des années 2000, une large harmonisation des dispositions nationales relatives à ces produits. Considérés comme aliments, leur nature particulière nécessite cependant une approche adaptative de la part du législateur européen. Cette nouvelle approche de l’aliment par le droit, favorable à la reconnaissance d’une santé alimentaire, tant convoitée par la société contemporaine, ne résout toutefois pas l’ambiguïté quant à la place à accorder aux « produits-frontière » dans le corpus juridique de l’Union européenne.Doctorat en Sciences juridiques
info:eu-repo/semantics/nonPublished
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VOS, Ellen. « Institutional frameworks of Community health and safety regulation : committees agencies and private bodies ». Doctoral thesis, 1997. http://hdl.handle.net/1814/4819.
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Defence date: 20 May 1997Examining board: Prof. R. Barents (Luxembourg/Maastricht) ; Prof. R. Dehousse (Florence), co-supervisor ; Prof. Ch. Joerges (Bremen/Florence), supervisor ; Judje P.J.G. Kapteyn (Luxembourg)
PDF of thesis uploaded from the Library digitised archive of EUI PhD theses completed between 2013 and 2017
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PELTONEN, Ellinoora. « Private control instruments in the European consumer, occupational health and safety, and environmental policies ». Doctoral thesis, 2010. http://hdl.handle.net/1814/15407.
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Defence Date: 06 December 2010Examining Board: Fabrizio CAFAGGI (Supervisor, EUI); Christian JOERGES (former EUI/University of Bremen); Colin SCOTT (University College, Dublin); Jyrki TALA (University of Turku and National Research Institute of Legal Policy, Helsinki)
PDF of thesis uploaded from the Library digital archive of EUI PhD theses
European Union’s (EU) legislature allows for EU level private interest governments (PIGs): stakeholders, industry, professional and co-operative bodies; and control entrepreneurs (PriCEs) to complement regulatory strategies. However, governance studies have infrequently conducted cross-sector analysis on how they assist in implementing EU policies. This study conducts cross-sector analysis of private compliance instruments (PCIs) utilised as partial implementing strategy to EU’s business regulation across consumer, worker health, safety and environmental policies. It introduces several opportunities to learn from differences. PriCEs appear operational PCIs throughout several legislative and private regulatory frameworks; regulatory sectors; targeting sector- or business-specific compliance; and employing either command-and-control or reflexive/responsive regulatory modes. However, workable 'in-house' PCIs implemented by PIGs necessitate specific market architecture and legislative pressure. Within sectors of health and safety of consumers and workers specific conditions may support in-house PCIs, which control business-specific compliance within command-and-control mode. However, within environmental sector, such in-house PCIs appear unfeasible. The EU legislature has also architected PCIs, which somewhat equate to reflexive/responsive mode, to consumer and environmental policies, whilst it has abstained from introduction of such instruments to worker health and safety due to autonomous social dialogue. Generally, at EU level, the potential for using outfitted reflexive mode PCIs appears greater than employing command-and-control mode in CPIs.
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ZUREK, Karolina. « European food regulation after enlargement : should Europe's modes of regulation provide for more flexibility ? » Doctoral thesis, 2010. http://hdl.handle.net/1814/14530.
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Defence date: 25 June 2010Examining Board: Mads Andenas (University of Oslo); Marise Cremona (EUI); Christian Joerges (Supervisor, former EUI and University of Bremen); Ellen Vos (University of Maastricht)
PDF of thesis uploaded from the Library digital archive of EUI PhD theses
This thesis aims to present a critical legal perspective on the current direction of European Union (EU) food safety regulation. Through an analysis of three regulatory mechanismsmutual recognition, scientific risk analysis and standardisation-combined with a study of the evolution of food legislation in the EU, I seek to show how the current framework fails to face new challenges, such as the globalization of world trade and the last two enlargements. In particular, the thesis focuses upon the case of a newly acceded EU member state, namely Poland. The main argument presented in the thesis is that an enlarged and more diversified Europe must not disregard the numerous socio-economic implications of market regulation. If not properly acknowledged and reflected in the regulatory scheme, the mismatch between market regulation and socio-economic factors can lead to a kind of gradual "disembedding" of the regulatory framework, in the Polanyian sense of the term. This is of critical importance as the EU project is not one-dimensionally geared towards securing greater European unity, but equally concerned with preserving unique European diversity-in the field of food as well as in other aspects. I am thus suggesting that the existing regulatory approach can be opened up to include a wider set of relevant socio-economic implications, allowing for protection of diversity while aiming for greater homogeneity. The legal system for the regulation of food can be rebalanced to become more flexible and responsive by shifting the use of existing regulatory mechanisms, in order to diversify regulatory intervention. First, this would require improvement of application of the risk analysis model, in order to guarantee inclusion of valid socio-economic concerns in the decision-making process. Second, it would also entail reliance on managed mutual recognition in those areas where protection of diversity does not collide with protection of consumers (for example, where either longstanding trust has been available or national codes have provided sufficient safety guarantees), and where consequently imposition of strict standardization is not necessary. Due to legitimate concerns with crisis, the regulatory framework for food in Europe has generated a bias against diversity leading to unforeseen and unintended consequences. This thesis argues that this need not be so.
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WIEHE, Reinhard. « Nachmarktkontrolle durch privatrechtlich-indirekte Steuerung : Eine ökonomisch orientierte Betrachtung ». Doctoral thesis, 1988. http://hdl.handle.net/1814/5615.
Texte intégralLivres sur le sujet "Product safety – Law and legislation – European Union countries"
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Institutional frameworks of community health and safety legislation : Committees, agencies, and private bodies. Oxford : Hart Pub., 1999.
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Dictionary of definitions of EU regulated products. The Hague : Kluwer Law Internattional, 1999.
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Fitzsimmons, Anthony. Insurance competition law : A handbook to the competition law of the European Union and the European Economic Area. London : Graham & Trotman/M. Nijhoff, 1994.
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EU chemicals regulation : New governance, hybridity and reach. Cheltenham, UK : Edward Elgar Publishing, 2015.
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1951-, Baldwin Robert, Daintith Terence et University of London. Institute of Advanced Legal Studies., dir. Harmonization and hazard : regulating health and safety in the European workplace. London : Graham & Trotman, 1992.
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The concept of the relevant product market : Between demand-side substitutability and supply-side substitutability in competition law. Frankfurt am Main : P. Lang, 2008.
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Associates, Peter Fisk. Chemical risk assessment : A manual for REACH. Chichester, West Sussex, United Kingdom : Wiley, 2014.
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Eriksson, Johan. Regulating Chemical Risks : European and Global Challenges. Dordrecht : Springer Science+Business Media B.V., 2010.
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Transatlantic regulatory cooperation : The shifting roles of the EU, the US and California. Cheltenham : Edward Elgar, 2011.
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Vos, Ellen. Institutional Frameworks of Community Health and Safety Legislation : Committees, Agencies and Private Bodies. Hart Publishing (UK), 1998.
Trouver le texte intégralChapitres de livres sur le sujet "Product safety – Law and legislation – European Union countries"
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Howells, Geraint. « 22. European consumer law ». Dans European Union Law, 704–30. Oxford University Press, 2020. http://dx.doi.org/10.1093/he/9780198855750.003.0022.
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This chapter examines EU consumer law. It discusses the negative impact of EU law on national consumer protection rules; rules on information duties (including the duty to not mislead) and the right of withdrawal; rules establishing consumer expectations; rules on product safety and product liability; and rules on unfair terms and sale of goods. The chapter also covers EU legislation providing general substantive rights; enforcement of consumer protection rules; and consumers’ right of private redress.
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Howells, Geraint. « 23. European consumer law ». Dans European Union Law. Oxford University Press, 2017. http://dx.doi.org/10.1093/he/9780198789130.003.0023.
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This chapter examines EU consumer law. It discusses the negative impact of EU law on national consumer protection rules; rules on information duties (including the duty to not mislead) and the right of withdrawal; rules establishing consumer expectations; rules on product safety and product liability; and rules on unfair terms and sale of goods. The chapter also covers EU legislation providing general substantive rights; enforcement of consumer protection rules; and consumers’ right of private redress.
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Kirk, Stephen. « Testing and More Testing – The Science Behind Keeping Your Skin Safe and Healthy ». Dans Discovering Cosmetic Science, 262–89. The Royal Society of Chemistry, 2020. http://dx.doi.org/10.1039/bk9781782624721-00262.
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This aim of this chapter is to give an insight into the philosophy and processes that are used to enable a cosmetic product to be placed on the market by a brand or high-street retailer. The European Union leads the world on cosmetic safety and efficacy legislation and this is being adopted by increasingly more countries around the world for their own. This can only be better for protecting the health and wellbeing of global cosmetic users.
Actes de conférences sur le sujet "Product safety – Law and legislation – European Union countries"
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Silovs, Mihails, et Olga Dmitrijeva. « Differences in fishery and aquaculture products, their production and sale technical regulations in Eurasian Economic Union and legislation and practice of the European Union ». Dans 22nd International Scientific Conference. “Economic Science for Rural Development 2021”. Latvia University of Life Sciences and Technologies. Faculty of Economics and Social Development, 2021. http://dx.doi.org/10.22616/esrd.2021.55.052.
Texte intégralRésumé :
The mandatory requirements for the fishery and aquaculture products, their production and sale in force in the territory of the Customs Union of the Eurasian Economic Union (CU EAEU) arise from the regulatory and legal acts of the Eurasian Economic Union and its predecessor - the Customs Union - and apply in a package approach similar to the law of the European Union pertaining to the food safety area. The requirements of the EAEU technical regulations have been analysed taking into account that European exporting enterprises are first of all obliged to comply with the requirements of the listed EU regulatory and legal acts applicable to their production process and products. The aim of this paper was to run a comparative analysis on the mandatory requirements of the food legislation of the European and Customs Unions regarding fishery and aquaculture products, their production and sale. The issues of certification of certain product categories are analysed separately, the requirements for canned fish being highlighted. The analysis is relevant for all fish processing companies which may consider the possibility of starting export to the countries of the CU EAEU and are intended to reduce costs associated with products’ entry into these markets.