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CDR Information Session for the Pharmaceutical Industry

le 21 octobre 2005

Agenda

Speakers’ Presentations

Introduction and welcome
Raymonde D’Amour, Facilitator

Evaluation of the Common Drug Review
Mike Tierney, Director, CDR

Proposed changes to the CDR Procedure
Elaine MacPhail, Program Advisor, CDR

Filing submissions – manufacturers’ comments on reviews
Sandra Pagotto, Manager, CDR Drug Reviews

Proposed changes to pharmacoeconomic requirements
Karen Lee, Health Economist, CDR

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