EMEA: Draft guideline on the conduct of bioequivalence studies for veterinary medicinal products
25.03.2009
EMEA:
Draft guideline on the conduct of bioequivalence studies for veterinary medicinal products. The aim of this guideline is to provide guidance regarding study design, conduct and evaluation including statistical considerations and acceptance limits for bioequivalence studies and in-vitro dissolution tests.
Draft guideline on the conduct of bioequivalence studies for veterinary medicinal products. The aim of this guideline is to provide guidance regarding study design, conduct and evaluation including statistical considerations and acceptance limits for bioequivalence studies and in-vitro dissolution tests.
The source of the news: http://www.emea.europa.eu/pdfs/vet/ewp/001600endraft.pdf
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