Human medicines European public assessment report (EPAR): DuoPlavin, clopidogrel,acetylsalicylic acid, Date of authorisation: 14/03/2010, Revision: 31, Status: Authorised

Human medicines European public assessment report (EPAR): DuoPlavin, clopidogrel,acetylsalicylic acid, Date of authorisation: 14/03/2010, Revision: 31, Status: Authorised

Training session for patients, consumers and healthcare professionals involved in medicine regulatory activities, Online, European Medicines Agency, Amsterdam, the Netherlands, from 5 December 2024, 14:00 (CET) to 13 December 2024, 12:00 (CET)

Training session for patients, consumers and healthcare professionals involved in medicine regulatory activities, Online, European Medicines Agency, Amsterdam, the Netherlands, from 5 December 2024, 14:00 (CET) to 13 December 2024, 12:00 (CET)

Opinion/decision on a Paediatric investigation plan (PIP): Ultomiris, ravulizumab, decision type: PM: decision on the application for modification of an agreed PIP, therapeutic area: Haematology-Hemostaseology;Uro-nephrology, PIP number: P/0128/2023

Opinion/decision on a Paediatric investigation plan (PIP): Ultomiris, ravulizumab, decision type: PM: decision on the application for modification of an agreed PIP, therapeutic area: Haematology-Hemostaseology;Uro-nephrology, PIP number: P/0128/2023

Opinion/decision on a Paediatric investigation plan (PIP): Dovato, lamivudine,dolutegravir, decision type: PM: decision on the application for modification of an agreed PIP, therapeutic area: Infectious diseases, PIP number: P/0121/2023

Opinion/decision on a Paediatric investigation plan (PIP): Dovato, lamivudine,dolutegravir, decision type: PM: decision on the application for modification of an agreed PIP, therapeutic area: Infectious diseases, PIP number: P/0121/2023

Newsletters

Stay informed on our latest news!

CAPTCHA

This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.