Using risk-based approaches across the product lifecycle to simplify, standardise & enhance the collection of safety data

Presentations
21/09/16

Dr. Rut explores the product lifecycle and reviews the areas of pharmacovigilance focus and opportunities for improvement for each: • Clinical studies – Maximising intelligence based on limited data • New to market – Establishing safety profile • On Patent Product – License maintenance • Off Patent / OTC – Efficiency and automation

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