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 Agency currently publishes for both centrally and non-centrally authorised medicines, as well as publication times and location on EMA’s website. It aims to help stakeholders know what kind of information to expect on medicines undergoing evaluations and other regulatory procedures.
More information on the EMA Website.
OpenEdition vous propose de citer ce billet de la manière suivante :
vroby (19 octobre 2024). EMA – Publication of a Guide to information on human medicines evaluated by European Medicines Agency: what the Agency publishes and when. ELSIBI. Consulté le 16 mars 2026 à l’adresse https://doi.org/10.58079/12j9m





