Human medicines European public assessment report (EPAR): ProQuad, measles, mumps, rubella and varicella vaccine (live), Date of authorisation: 05/04/2006, Revision: 36, Status: Authorised
Human medicines European public assessment report (EPAR): Riulvy, tegomil fumarate, Date of authorisation: 28/07/2025, Revision: 1, Status: Authorised
Pharmacovigilance-related regulatory recommendations for centrally authorised veterinary medicinal products during 2025
Product-specific bioequivalence guidance
Eltrombopag film-coated tablets 12.5 mg, 25 mg, 50 mg, 75 mg and powder for oral suspension 25 mg product-specific bioequivalence guidance
Melatonin prolonged release tablets 2 mg product-specific bioequivalence guidance
Members of the Coordinating group of European network of paediatric research at the European Medicines Agency (Enpr-EMA)
Procedural advice on publication of information on withdrawals of marketing authorisation and variation applications for veterinary medicinal products
New co-chairs elected for working parties for healthcare professionals and for patients and consumers
Timetable: Post-authorisation measure (PAM) assessed by PRAC