The eAF newsletter is published four times a year and provides pharmaceutical companies and the national competent authorities in the EU with updates on the progress of the web-based eAF and PMS.
This third issue covers topics such as:
You can find the complete third issue of the newsletter here.
For further information, contact us at: [email protected]
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The transition period for the EU Regulation on Clinical Trials on medicinal products for human use (CTR, 536/2014) is approaching its conclusion, with a final
El objetivo del curso es ofrecer una actualización de la normativa y los sistemas telemáticos para la gestión de la información de los medicamentos de uso humano con las autoridades sanitarias.
Last week, during the Q3 System Demo, the EMA shared important updates: During this Q4 2024, the PUI (Product User Interface) will be released, enabling
Services
Memberships & Partnerships
Quality Management System
SDGs
As a company committed to sustainability, we follow the UN’s 2030 Agenda and its Sustainable Development Goals.
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