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Draft Note Guidance Investigation Bioavailability ...

The European Agency for the Evaluation of Medicinal Products Evaluation of Medicines for Human Use London, 14 December 2000. CPMP/EWP/QWP/1401/98. COMMITTEE FOR PROPRIETARY MEDICINAL PRODUCTS. (CPMP). NOTE FOR Guidance ON. THE Investigation OF Bioavailability AND. BIOEQUIVALENCE. DISCUSSION IN THE JOINT EFFICACY AND QUALITY December 1997- WORKING GROUP October 1998. TRANSMISSION TO THE CPMP July 1998. RELEASE FOR CONSULTATION December 1998. DEADLINE FOR COMMENTS June 1999. DISCUSSION IN THE DRAFTING GROUP February May 2000.

INVESTIGATION OF BIOAVAILABILITY AND BIOEQUIVALENCE TABLE OF CONTENTS 1 INTRODUCTION 2 ... 3 action in an effective concentration for the desired period. To allow reliable prediction of the ... 74 more practical definition can then be given, taking into consideration that the substance in the

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