Challenges of using pluripotent stem cells for safety assessments of substances

Author:

Vojnits Kinga,Bremer Susanne

Publisher

Elsevier BV

Subject

Toxicology

Reference68 articles.

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2. Anon., 2003a. EGE Opinion on the ethical aspects of clinical research in developing countries. http://ec.europa.eu/european_group_ethics/docs/avis17_complet_en.pdf, accessed (25.2.2009).

3. Anon., 2003b. Directive 2003/15/EC of the European Parliament and of the Council of 27 February 2003 amending Council Directive 76/768/EEC on the approximation of the laws of the Member States relating to cosmetic products. Official Journal of the European Union 11.3.2003 L66/26; http://europa.eu/eur-lex/pri/en/oj/dat/2003/l_066/l_06620030311en00260035.pdf, accessed (25.5.2009).

4. Anon., 2006a. International Society for Stem Cell Research Guidelines for the Conduct of Human Embryonic Stem Cell Research. International Society for Stem Cell Research, Illinois, USA 2006; http://www.isscr.org/guidelines/ISSCRhESCguidelines2006.pdf, accessed (25.2.2009).

5. Anon., 2006b. Decision No 1982/2006/EC of the European Parliament and of the Council of 18 December 2006 concerning the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007–2013) Art. 6 Official Journal of the European Union L 412/5; http://eur-lex.europa.eu/LexUriServ/site/en/oj/2006/l_412/l_41220061230en00010041.pdf, accessed (25.5.2009).

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