Agenda
9:00 AM — 10:30 AM
IMPLICATIONS OF THE NEW PHARMACOVIGILANCE LEGISLATION11:00 AM — 12:30 PM
RISK MANAGEMENT PLANS4:00 PM — 5:30 PM
CLINICAL TRIAL REGISTRIES9:00 AM — 10:30 AM
REGIONAL CONSIDERATIONS11:00 AM — 12:30 PM
STORYLINE DOCUMENTS2:00 PM — 3:30 PM
SUBMISSION CHALLENGES4:00 PM — 5:30 PM
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