EU legislations affecting safety data availability of cosmetic ingredients

Author:

Pauwels Marleen,Rogiers Vera

Publisher

Elsevier BV

Subject

Toxicology,General Medicine

Reference30 articles.

1. ECB, 2003. European Chemicals Bureau. Technical Guidance Document on Risk Assessment in support of Commission Directive 93/67/EEC on Risk Assessment for new notified substances, Commission Regulation (EC) No 1488/94 on Risk Assessment for existing substances and Directive 98/8/EC of the European Parliament and of the Council Concerning the Placing of Biocidal Products on the Market. Doc. EUR 20418 EN/1, European Communities (2003).

2. ECVAM, 2007. Report from the Commission to the Council and the European Parliament—Report on the Development, Validation and Legal Acceptance of Alternative Methods to Animal Tests in the Field of Cosmetics (2005). Cosmetics Technical report drafted by ECVAM in 2005/2006 in support of the preparation of the above report. Available from: (Consulted July 2007).

3. EMEA (European Agency for the Evaluation of Medicinal Products), 2006. Guidance Document on Non-clinical Day 80 Assessment Report. Revision 2. Available from: . (Consulted July 2007).

4. Alternative (non-animal) methods for cosmetic testing: current status and future prospects;Eskes;ATLA,2005

5. EU, 1965. Council Directive 65/65/EEC of 26 January 1965 on the approximation of provisions laid down by law, regulation or administrative action relating to proprietary medicinal products. OJ 022, 369–373, 9 February 1965.

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