Regulatory demands on data quality for the environmental risk assessment of pharmaceuticals-Reference-Cited by-同舟云学术

Regulatory demands on data quality for the environmental risk assessment of pharmaceuticals

Published:2009-12 Issue:3 Volume:55 Page:276-280
ISSN:0273-2300
Container-title:Regulatory Toxicology and Pharmacology
language:en
Short-container-title:Regulatory Toxicology and Pharmacology

Author:

Küster A.,Bachmann J.,Brandt U.,Ebert I.,Hickmann S.,Klein-Goedicke J.,Maack G.,Schmitz S.,Thumm E.,Rechenberg B.

Publisher

Elsevier BV

Subject

Toxicology,General Medicine

Reference7 articles.

1. VICH, 2000. Guideline on environmental impact assessment (EIAS) for veterinary medicinal products – Phase I. VICH Topic GL6. International cooperation on harmonisation of technical requirements for registration of veterinary medicinal products.

2. VICH, 2004. Guideline on environmental impact assessment for veterinary medicinal products – Phase II. VICH Topic GL38. International cooperation on harmonisation of technical requirements for registration of veterinary medicinal products.

3. EMEA, 2006. Guideline on the environmental risk assessment of medicinal products for human use. European Medicines Evaluation Agency. Doc.Ref.EMEA/CHMP/SWP/4447/00.

4. EMEA, 2007. Guideline on environmental impact assessment for veterinary medicinal products in support of the VICH guidelines GL6 and GL38. European Medicines Agency. Committee for medicinal products for veterinary use (CVMP). EMEA/CVMP/ERA/418282/2005-Corr.

5. EMEA, 2008a. Revised Guideline on environmental impact assessment for veterinary medicinal products in support of the VICH guidelines GL6 and GL38. European Medicines Agency. Committee for Medicinal Products for Veterinary Use (CVMP). EMEA/CVMP/ERA/418282/2005-Rev.1, 17 Nov. 2008.

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