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© World Health Organization WHO Technical Report Series, No. 937, 2006 Annex 9 Additional guidance for organizations performing in vivo bioequivalence studies
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Document Date: 2006-11-21 08:38:02


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City

Geneva / Helsinki / /

Company

Archive / /

Event

FDA Phase / /

Facility

Clinical laboratory Personnel Quality / /

IndustryTerm

multisource product / multisource drug product / pharmaceutical product / study site / active pharmaceutical ingredient / word processing / comparator product / investigational product / Self-designed software programs / study protocols / data management / test product / manufacturing practices / trial protocol / software programs / trial site / manufacturing sites / office equipment / study product / pharmaceutical products / magnetic media / medicinal products / optical media / pharmaceutical operations / pharmaceutical alternative / /

Organization

World Health Organization / Organisation for Economic Co-operation and Development / Glossary Organization / /

Position

investigator / coordinator / investigator / the institution involved and the sponsor / director According to / principal investigator The investigator / /

Product

Annexs6-9 / /

Technology

pharmacokinetics / study protocols / trial protocol / agreed protocol / /

URL

http /

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