The Veterinary Medicines Directorate (VMD) has launched a new digital service for reporting adverse events associated with animal medicines, making it easier for veterinary professionals and animal owners to submit reports directly to the regulator.
Version 1.28.0.0 of the Human Marketing Authorisation Application (MAA) electronic Application Form (eAF) is now available. Industry
On 30 June, we reached a major regulatory milestone. At Asphalion, we supported some leading international pharmaceutical
This practical seminar is aimed at anyone involved in planning, creating or submitting variations.
This week, our regulatory experts, Maria Castellà and Alejandro Ballester, participated in the first consortium meeting of
Hoy, 30 de junio de 2026, finaliza el plazo de registro de alérgenos del Grupo II (ácaros).
The objective of this project is to create a siRNA-combined advanced therapy, which will allow a more personalised treatment for the different stages of osteoarthritis. All siNPAIN partners are working hard to develop an efficient therapy to improve the quality of life of those affected by osteoarthritis, a chronic joint condition that affects more and more people every year.
Are You Ready for a Pharmacovigilance Inspection? Being inspection-ready means more than preparing when a notification arrives.
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Schedule here a free 30-minutes meeting with one of our consultants and tell us about your project, challenges or doubts.
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