EMA - Publication of a Guide to information on human medicines evaluated by European Medicines Agency: what the Agency publishes and when

The EMA issued a new Guide to information on human medicines evaluated by European Medicines Agency: what the Agency publishes and when. The European Medicines Agency (EMA) publishes information on human medicinal products at various stages of their life cycle, from the early developmental stages through to EMA’s evaluation of authorisation applications, post-authorisation changes, safety reviews and withdrawals of authorisation. This guide describes the different types of information the Ag...