NHC training sessions | Key aspects of the reform of EU pharmaceutical legislation
The reform of EU pharmaceutical legislation represents one of the most significant transformations of the regulatory framework
October 23, 2026
The reform of EU pharmaceutical legislation represents one of the most significant transformations of the regulatory framework
El próximo 22 de octubre, nuestra compañera Ana Viñas participará en el curso especializado en Registros en
MHRA announces changes to the International Recognition Procedure (IRP)
The Spanish Agency of Medicines and Medical Devices (AEMPS) has announced that it will no longer issue
Version 1.28.0.0 of the Human Marketing Authorisation Application (MAA) electronic Application Form (eAF) is now available. Industry
This practical seminar is aimed at anyone involved in planning, creating or submitting variations.
Hoy, 30 de junio de 2026, finaliza el plazo de registro de alérgenos del Grupo II (ácaros).
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