European Medicines Agency (EMA) MEMBER COUNTRIES

European Shortages Monitoring Platform (ESMP) training on CAP routine shortage reporting for MAHsПодробнее

ESMP Essentials and Industry Reporting Requirements Webinar - 24 June 2024Подробнее

How does EMA ensure the safety of medicines in the EUПодробнее

Session 3: Prevention of shortagesПодробнее

Overview of the European Medicines Agency (EMA), Part 1 of 3Подробнее

DRUG APPROVAL PROCESS IN EUROPE I EMA I NATIONAL AUTHORISATION PROCEDURE I PART II IПодробнее

Session 6: Contribution of EMA and the EU network to veterinary medicinesПодробнее

Drug regulatory BodiesПодробнее

Session 1: A new veterinary medicines regulation - one year in operationПодробнее

EMA press briefing 11 January 2022Подробнее

What Is the European Medicines Agency (EMA)? What Is its Role?Подробнее

EMA press briefing 3 February 2022Подробнее

EU calls on members to join forces on rolling out drugs. Health commissioner EU debatesПодробнее

EU Marketing Authorisation | What are the Steps and Timelines for Centralised Procedure at EMA?| DRAПодробнее

EU drug regulator EMA advises members to make their own decisions on AstraZeneca vaccineПодробнее

MARKETING AUTHORIZATION APPLICATION PROCEDURES | MAA | EUROPE | REGULATORY AFFAIRSПодробнее

European Medicine Agency Overview Regulatory Lectures by Rajashri Ojha at Raaj Pharma e-learningПодробнее

EMA / FVE Webinar on AMEG categorisationПодробнее

EMA press briefing 28 May 2021Подробнее