Showing papers on "Legislation published in 2022"

A Review on Global E-Waste Management: Urban Mining towards a Sustainable Future and Circular Economy

Abstract: The trending need for smarter electrical and electronic equipment (EEE) is surging globally by the year and is giving rise to huge amounts of outdated EEE going into landfills. This has caused enormous threats to our environment and the health of living beings due to its unsustainable ways of collection, treatment and disposal of waste EEE or E-waste. With increasing E-waste, the formal sectors lack infrastructure, technology and expertise required to collect and process the E-waste in an environmentally sound manner. This article is intended to bring out the global best practices in the field of E-waste management, to shed light on the importance of policy implementation, technology requirement and social awareness to arrive at a sustainable and circular economy. Although about 71% of the world’s populace has incorporated E-waste legislation, there is a need to enforce and implement a common legal framework across the globe. The article explains the gap created among the stakeholders and their knowledge on the roles and responsibilities towards a legalized E-waste management. It further explains the lack of awareness on extended producer responsibility (EPR) and producer responsibility schemes. Despite various legislations in force, numerous illegal practices such as acid leaching, open incineration, illegal dumping carried out by the informal sector are causing harm to the environment, natural resources and the safety of unorganized and unskilled labor. The article discusses the crucial need for awareness amongst stakeholders, consumer behavior and the global challenges and opportunities in this field to achieve a low-carbon, circular economy. To conclude, the article highlights the importance of common legal framework, EPR and licenses, transformation of the informal sector, benchmark technologies, responsibilities of various stakeholders and entrepreneurial opportunities to enhance the formal capacity. The article wholly advocates for transparency, accountability and traceability in the E-waste recycling chain, thus creating a greener environment and protecting our planet and natural resources for future generations.

Review of the evidence of sentience in cephalopod molluscs and decapod crustaceans

Abstract: All cephalopod molluscs and decapod crustaceans should be regarded as sentient and protected under UK animal welfare law. This is the headline conclusion of this thoughtful report, that is going to have a profound impact on the way these animals are treated within the UK — and likely inform policy elsewhere. In response, the UK government has indicated that they accept this position and will look to/have extended forthcoming animal welfare legislation to include lobsters, octopus and crabs and all other decapod crustaceans and cephalopod molluscs.

Packaging and the Environment

Abstract: The leading book on packaging and the environment-now expanded and updated This is a detailed examination and objective analysis of all aspects of environmental problems related to packaging: resource depletion, pollution, solid waste management, recycling, degradability, package design considerations, and legislation. The author is a leading authority on the subject. The presentation is well documented and non-partisan. This new edition is expanded and completely updated.

Algae as Food in Europe: An Overview of Species Diversity and Their Application

Abstract: Algae have been consumed for millennia in several parts of the world as food, food supplements, and additives, due to their unique organoleptic properties and nutritional and health benefits. Algae are sustainable sources of proteins, minerals, and fiber, with well-balanced essential amino acids, pigments, and fatty acids, among other relevant metabolites for human nutrition. This review covers the historical consumption of algae in Europe, developments in the current European market, challenges when introducing new species to the market, bottlenecks in production technology, consumer acceptance, and legislation. The current algae species that are consumed and commercialized in Europe were investigated, according to their status under the European Union (EU) Novel Food legislation, along with the market perspectives in terms of the current research and development initiatives, while evaluating the interest and potential in the European market. The regular consumption of more than 150 algae species was identified, of which only 20% are approved under the EU Novel Food legislation, which demonstrates that the current legislation is not broad enough and requires an urgent update. Finally, the potential of the European algae market growth was indicated by the analysis of the trends in research, technological advances, and market initiatives to promote algae commercialization and consumption.

Anti-Transgender Legislation—A Public Health Concern for Transgender Youth

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The 2020 European Union report on pesticide residues in food

Abstract: Abstract Under European Union legislation (Article 32, Regulation (EC) No 396/2005), the EFSA provides an annual report which examines pesticide residue levels in foods on the European market. This report is based on data from the official national control activities carried out by EU Member States, Iceland and Norway and includes a subset of data from the EU‐coordinated control programme, which uses a randomised sampling strategy. For 2020, 94.9% of the overall 88,141 samples analysed fell below the maximum residue level (MRL), 5.1% exceeded this level, of which 3.6% were non‐compliant, i.e. samples exceeding the MRL after taking the measurement uncertainty into account. For the subset of 12,077 samples analysed as part of the EU‐coordinated multiannual control programme, 1.7% exceeded the MRL and 0.9% were non‐compliant. To assess acute and chronic risk to consumer health, dietary exposure to pesticide residues was estimated and compared with health‐based guidance values. Dietary exposure to pesticides for which health‐based guidance values were available is unlikely to pose a risk to EU consumer health. In the rare cases where dietary exposure for a specific pesticide/product combination was calculated to exceed the health‐based guidance value, and for those pesticides for which no health‐based guidance value could be established, the competent authorities took appropriate and proportionate corrective measures to address potential risks to consumers. Recommendations are proposed to increase the effectiveness of European control systems, thereby continuing to ensure a high level of consumer protection throughout the EU.

Post-market surveillance of medical devices: A review.

Abstract: BACKGROUND Medical devices (MDs) represent the backbone of the modern healthcare system. Considering their importance in daily medical practice, the process of manufacturing, marketing and usage has to be regulated at all levels. Harmonized evidence-based conformity assessment of MDs during PMS relying on traceability of medical device measurements can contribute to higher reliability of MD performance and consequently to higher reliability of diagnosis and treatments. OBJECTIVE This paper discusses issues within MD post-market surveillance (PMS) mechanisms in order to set a path to harmonization of MD PMS. METHODS Medline (1980-2021), EBSCO (1991-2021), and PubMed (1980-2021) as well as national and international legislation and standard databases along with reference lists of eligible articles and guidelines of relevant regulatory authorities such as European Commission, Food and Drug Administration were searched for relevant information. Journal articles that contain information regarding PMS methodologies concerning stand-alone medical devices. National and international legislation, standards and guidelines concerning the topic. RESULTS The search strategy resulted in 2282 papers. Out of those only 24 articles satisfied the eligibility criteria and were finally included in the review. Papers were grouped per categories: medical device registry, medical device adverse event reporting, and medical device performance evaluation. In addition to journal articles, national and international legislation, standards, and guidelines were reviewed to assess the state of PMS in different regions of the world. CONCLUSION Although the regulatory framework prescribes PMS of medical devices, the process itself is not harmonized with international standards. Particularly, conformity assessment of MDs, as an important part of PMS, is not measured and managed in a traceable, evidence-based manner. The lack of harmonization within PMS results in an environment of increased adverse events involving MDs and overall mistrust in medical device diagnosis and treatment results.

A Short History of South Africa

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Do Firms Respond to Gender Pay Gap Transparency?

Abstract: We examine the effect of pay transparency on the gender pay gap and firm outcomes. Using a 2006 legislation change in Denmark that requires firms to provide gender-disaggregated wage statistics, detailed employee-employer administrative data, and difference-in-differences and difference-in-discontinuities designs, we find that the law reduces the gender pay gap, primarily by slowing wage growth for male employees. The gender pay gap declines by two percentage points, or 13% relative to the pre-legislation mean. Despite the reduction of the overall wage bill, the wage transparency mandate does not affect firm profitability, likely because of the offsetting effect of reduced firm productivity. This article is protected by copyright. All rights reserved

OUP accepted manuscript

Abstract: In April 2021, the 5th German REACH Congress took place as a hybrid event with a focus on discussing interlinkages between REACH and the occupational safety and health (OSH) legislation. More than 1000 people from Germany, the EU, and non-EU countries representing all stakeholder groups participated via livestream. Around 10% of the participants provided their opinions on various issues in an online survey. The presentations and discussions, as well as the results of the online survey, show that the stakeholders perceive a positive effect of REACH on the implementation of OSH, in particular via the information made available through the registration and communication in the supply chain, and the restrictions and authorization procedures. The integration of OSH and REACH expertise in the regulatory processes, as well as transparency and clarity about the selection of regulatory instruments to manage workplace risks, were highlighted as areas for potential improvement. Overall, it was concluded that the Chemicals Strategy for Sustainability would further improve the interplay of legislation, which would also benefit the level of safety and health at workplaces.

E-commerce and its limits in the context of the consumer protection: the case of the Slovak Republic

Abstract: The COVID-19 pandemic and lockdowns resulted in an unusual increase in electronic commerce not only in the conditions of the Slovak Republic. This fact also causes many unanswered questions in business practice, which bother entrepreneurs in ecommerce, especially in the context of consumer protection. The main goal of the article is to examine the current possibilities of electronic commerce in the conditions of the Slovak Republic and especially its limits in the context of consumer protection as a weaker part. Determining the goal of a scientific studye conceived in this way responds to the current practical problems in the business practice. Due to the nature of the researched topic, we have applied analysis, synthesis as well as comparison of legal regulations in the processing of this issue. However, in addition to the mentioned scientific methods of research, we also used scientific literature, case law and analogy of the law. In our scientific article, we strive for qualified answers to the needs of business practice. In conclusion, we critically point out the application problems we have identified and we proposed legislation.

Changes in cannabis policy and prevalence of recreational cannabis use among adolescents and young adults in Europe—An interrupted time-series analysis

Abstract: Background Cannabis policy varies greatly across European countries, but evidence of how such policy impacts on recreational cannabis use among young people is conflicting. This study aimed to clarify this association by investigating how changes in cannabis legislation influenced cannabis use. Methods Available data on self-reports of recreational cannabis use among individuals aged 15–34 years was retrieved from EMCDDA. Information on cannabis policy changes was categorized as more lenient (decriminalisation or depenalisation) or stricter (criminalisation, penalisation). Countries that had implemented changes in cannabis legislation or had information on prevalence of use for at least eight calendar years, were eligible for inclusion. We used interrupted time-series linear models to investigate changes in country-specific trajectories of prevalence over calendar time and in relation to policy changes. Results Data from Belgium, Czech Republic, Germany, Italy, Netherlands, Norway, Portugal, Slovakia, Spain, Sweden and United Kingdom, for 1994–2017 was available for analyses. Cannabis use varied considerably over the study period and between countries. On average, use was stable or weakly increasing in countries where legislation was not changed or changed at the extremes of the study period (+0.08 percent per year [95% CI -0.01, 0.17 percent]). In contrast, the pooled average use decreased after changes in legislation, regardless of whether it had become more lenient (-0.22 [-1.21, 0.77]) or stricter (-0.44 [-0.91, 0.03]). Conclusions Our findings do not support any considerable impact of cannabis legislation on the prevalence of recreational cannabis use among youth and young adults in Europe.

Recycling Plastics from WEEE: A Review of the Environmental and Human Health Challenges Associated with Brominated Flame Retardants

Abstract: Waste electrical and electronic equipment (WEEE) presents the dual characteristic of containing both hazardous substances and valuable recoverable materials. Mainly found in WEEE plastics, brominated flame retardants (BFRs) are a component of particular interest. Several actions have been taken worldwide to regulate their use and disposal, however, in countries where no regulation is in place, the recovery of highly valuable materials has promoted the development of informal treatment facilities, with serious consequences for the environment and the health of the workers and communities involved. Hence, in this review we examine a wide spectrum of aspects related to WEEE plastic management. A search of legislation and the literature was made to determine the current legal framework by region/country. Additionally, we focused on identifying the most relevant methods of existing industrial processes for determining BFRs and their challenges. BFR occurrence and substitution by novel BFRs (NBFRs) was reviewed. An emphasis was given to review the health and environmental impacts associated with BFR/NBFR presence in waste, consumer products, and WEEE recycling facilities. Knowledge and research gaps of this topic were highlighted. Finally, the discussion on current trends and proposals to attend to this relevant issue were outlined.

Quality Risk Management Approach for Drug Development and Its Future Prospectives

Abstract: These days, finding new marketing authorizations, guaranteeing regulatory compliance, and keeping labour costs competitive are extremely tough. Many pharmaceutical companies also struggle to deal with local regulatory issues and stay up with changes in key pharmaceutical markets. Regulations are thoroughly reviewed before being given to the RA department. This team compiles the most critical prescription information for global approval and marketing. This category accepts both new and revised product submissions. This is mostly handled by the RA department. RA's job is to provide feedback on proposed or disputed legislation. This is a proactive measure. The ICH framework allows for more early intervention. Regulators have a wide range of responsibilities. In the US, the FDA must register and clear the goods with the export company's regulatory professional.

A review of the recent development, challenges, and opportunities of electronic waste (e-waste)

Abstract: Abstract This study reviews recent developments, challenges, and the prospect of electronic waste (e-waste). Various aspects of e-waste, including collection, pre-treatment, and recycling, are discussed briefly. It is found that Europe is the leading collector of e-waste, followed by Asia, America, Oceania, and Africa. The monetary worth of e-waste raw materials is estimated to be $57.0 billion. However, only $10.0 billion worth of e-waste is recycled and recovered sustainably, offsetting 15.0 million tonnes (Mt) of CO 2 . The major challenges of e-waste treatment include collection, sorting and inhomogeneity of waste, low energy density, prevention of further waste, emission, and cost-effective recycling. Only 78 countries in the world now have e-waste related legislation. Such legislation is not effectively implemented in most regions. Developing countries like south-eastern Asia and Northern Africa have limited or no e-waste legislation. Therefore, country-specific standards and legislation, public awareness, effective implementation, and government incentives for developing cost-effective technologies are sought to manage e-waste, which will play an important role in the circular economy.

Should Per Se Limits Be Imposed For Cannabis? Equating Cannabinoid Blood Concentrations with Actual Driver Impairment: Practical Limitations and Concerns

Abstract: Fourteen US states have amended their longstanding, effect-based DUI drug laws to per se or zero tolerant per se statutes in regard to cannabis. Other states are considering enacting similar legislation. Under these amended traffic safety laws, it is a criminal violation for one to operate a motor vehicle with trace levels of cannabinoids or their metabolites in his or her blood or urine. Opponents of per se cannabinoid limits argue that neither the presence of cannabinoids nor their metabolites are appropriate or consistent predictors of behavioral or psychomotor impairment. They further argue that the imposition of such per se limits may result in the criminal conviction of individuals who may have previously consumed cannabis at some unspecified point in time, but were no longer under its influence. As more states enact statutory changes allowing for the legal use of cannabis under certain circumstances, there is a growing need to re-examine the appropriateness of these proposed per se standards for cannabinoids and their metabolites because the imposition of such limits may, in some instances, inadvertently criminalize behavior that poses no threat to traffic safety, such as the state-sanctioned private consumption of cannabis by adults.

Geographical Origin Assessment of Extra Virgin Olive Oil via NMR and MS Combined with Chemometrics as Analytical Approaches

Abstract: Geographical origin assessment of extra virgin olive oil (EVOO) is recognised worldwide as raising consumers’ awareness of product authenticity and the need to protect top-quality products. The need for geographical origin assessment is also related to mandatory legislation and/or the obligations of true labelling in some countries. Nevertheless, official methods for such specific authentication of EVOOs are still missing. Among the analytical techniques useful for certification of geographical origin, nuclear magnetic resonance (NMR) and mass spectroscopy (MS), combined with chemometrics, have been widely used. This review considers published works describing the use of these analytical methods, supported by statistical protocols such as multivariate analysis (MVA), for EVOO origin assessment. The research has shown that some specific countries, generally corresponding to the main worldwide producers, are more interested than others in origin assessment and certification. Some specific producers such as Italian EVOO producers may have been focused on this area because of consumers’ interest and/or intrinsic economical value, as testified also by the national concern on the topic. Both NMR- and MS-based approaches represent a mature field where a general validation method for EVOOs geographic origin assessment could be established as a reference recognised procedure.

Myths and Realities about Genetically Modified Food: A Risk-Benefit Analysis

Abstract: The development and consumption of genetically modified (GM) crops are surrounded by controversy. According to proponents, only molecular biology approaches and genetic engineering tools are realistic food shortage solutions for the world’s ever-growing population. The main purpose of this study is to review the impact of GM products on human, animal, and environmental health. People still reject GM crops not only because of safety concerns, but also for moral reasons. Toxicity, allergies, and possible horizontal gene transfer (HGT) to the environment or to other species have been associated with the marketing of GM products. Moreover, the scarce data available about the long-term implications of using GM crops is another opponent concern. Nevertheless, science has evidenced no harm from GM crops use to date but has, instead, reported several benefits that result from their commercialization, such as economic, environmental, and health benefits for the general public. Legislation and policies about GM product labeling standards are being discussed. To overcome emerging food security challenges, considering quality scientific information is essential rather than leaving the issue and merely moving toward moral discussion. Hence, a risk–benefit analysis is necessary.