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The prices below are industry pricing. Reduced pricing may be available for Nonprofit/Academia and Government, subject to eligibility verification. Click Register to get pricing appropriate for your work setting. Review the cancellation and transfer policy.
Related events
Fees
- EM01: HOT TOPICS IN PHARMACOVIGILANCE AND ADVERSE REACTION REPORTING €450
- EM02: INTERACTIONS BETWEEN REGULATORY AND INTELLECTUAL PROPERTY, PRODUCT LIABILITY AND DATA PRIVACY €450
- EM03: ANALYSIS OF SAFETY DATA FROM CLINICAL TRIALS €450
- EM04: PRIVACY AND PERSONAL DATA PROTECTION IN DRUG DEVELOPMENT €450
- EM05: MOVING FROM RISK MANAGEMENT TO BENEFIT/RISK MANAGEMENT - EMBEDDING PHARMACOVIGILANCE PRINCIPLES INTO THE PRODUCT LIFE CYCLE €450
- EM06: MODELLING AND SIMULATION (M&S) / MODEL INFORMED DRUG DISCOVERY AND DEVELOPMENT (MID3) €450
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