Legislation and Current Practices Concerning Risk Assessment of Skin Sensitizers in the European Union: A Comparative and Survey Study

IF 4.8 1区 医学 Q2 ALLERGY
Mathias Krogh Pedersen, Jakob Ferløv Baselius Schwensen, Jose Hernán Alfonso, Steen Mollerup, Gianluca Selvestrel, Christina Rudén, Martin F. Wilks, Jeanne Duus Johansen
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Abstract

Background

Despite legislation aimed to protect the population against skin sensitization in the European Union (EU), over one quarter of the general population is sensitised to at least one chemical.

Objectives

To provide an overview and comparison of European legislation concerning skin sensitization. In addition, we gathered the opinions of experts and stakeholders regarding improvements in the legislation and risk assessment process in the EU, to provide suggestions for improvement.

Methods

Legislation was identified and compared. Four questionnaires were created towards industry, competent authorities and regulators, researchers/clinicians, and non-governmental organisations. The questions concerned the legislation, the risk assessment process, data collection and potential improvements.

Results

Seven areas of legislation were analysed. The legislation was found to be unharmonised, for example, differing modes of restriction and accepted tests for skin sensitization. Approximately 40% of the questionnaire respondents found that the EU legislation and tools were not sufficiently protective. To improve the legislation 83% suggested harmonisation and 68% suggested better data sharing. Other areas were: improved exposure data (78%), better understanding of the skin sensitization mechanism (67%) and non-animal tests (66%).

Conclusions

Stakeholders had varying confidence towards the protection of European citizens against skin sensitization. Multiple areas for improvement regarding the legislations and the risk assessment process were identified.

Abstract Image

欧盟关于皮肤致敏剂风险评估的立法和现行做法:一项比较和调查研究。
背景:尽管欧盟立法旨在保护人群免受皮肤致敏,但超过四分之一的普通人群对至少一种化学物质敏感。目的:提供一个概述和比较有关皮肤致敏的欧洲立法。此外,我们收集了专家和利益相关者对欧盟立法和风险评估过程改进的意见,以提供改进建议。方法:进行立法鉴定和比较。针对行业、主管当局和监管机构、研究人员/临床医生和非政府组织创建了四份问卷。这些问题涉及立法、风险评估过程、数据收集和可能的改进。结果:分析了七个立法领域。立法被发现是不协调的,例如,不同的限制模式和可接受的皮肤致敏试验。大约40%的受访者认为欧盟的立法和工具保护力度不够。为了改善立法,83%的人建议协调一致,68%的人建议更好地共享数据。其他领域包括:改善暴露数据(78%),更好地了解皮肤致敏机制(67%)和非动物试验(66%)。结论:利益相关者对保护欧洲公民免受皮肤致敏有不同的信心。确定了有关立法和风险评估过程的多个有待改进的领域。
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来源期刊
Contact Dermatitis
Contact Dermatitis 医学-过敏
CiteScore
4.60
自引率
30.90%
发文量
227
审稿时长
4-8 weeks
期刊介绍: Contact Dermatitis is designed primarily as a journal for clinicians who are interested in various aspects of environmental dermatitis. This includes both allergic and irritant (toxic) types of contact dermatitis, occupational (industrial) dermatitis and consumers" dermatitis from such products as cosmetics and toiletries. The journal aims at promoting and maintaining communication among dermatologists, industrial physicians, allergists and clinical immunologists, as well as chemists and research workers involved in industry and the production of consumer goods. Papers are invited on clinical observations, diagnosis and methods of investigation of patients, therapeutic measures, organisation and legislation relating to the control of occupational and consumers".
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