The European Medicines Agency is a decentralised agency of the European Union responsible for the evaluation, supervision and safety monitoring of medicines.

The European Medicines Agency (EMA) facilitates development and access to medicines for countries within the European Union (EU). EMA evaluates applications for marketing authorisation submitted via the centralised procedure, monitors the safety of medicines across their lifecycle and provides information to healthcare professionals and patients.

The European Medicines Agency (EMA) is an agency of the European Union (EU) in charge of the evaluation and supervision of pharmaceutical products. Prior to 2004, it was known as the European Agency for the Evaluation of Medicinal Products or European Medicines Evaluation Agency (EMEA). [4] [5]

Jan 31, 2025 · The authorisation and oversight of clinical trials is the responsibility of EU/EEA Member States while EMA is responsible for maintaining the CTIS. The European Commission oversees the implementation of the Clinical Trials Regulation. Throughout 2025, the performance and the user experience of CTIS will continue to be improved.

The European Medicines Agency (EMA) protects and promotes human and animal health by evaluating and monitoring medicines within the European Union (EU) and the European Economic Area (EEA). The Agency's main responsibilities are authorising and monitoring medicines in the EU.

2 days ago · The European Medicines Agency (EMA) has implemented a strategy to accelerate drug approvals in the EU. Learn more about their initiatives and how they are streamlining the process for faster ...

Jan 27, 2025 · As part of EMA’s ongoing engagement efforts with IRIS users the regulatory procedure management team conducted a survey in 2024. The results suggest a majority of industry users are new to the system and not existing users. Prospective users seem to have been able to find their way to the various webinars about IRIS and they have bene able to ...

The European Medicines Agency (EMA) is a decentralised agency of the European Union (EU). It is responsible for the scientific evaluation, supervision and safety monitoring of medicines.

Jul 4, 2023 · What Is the European Medicines Agency (EMA)? The European Medicines Agency (EMA) is a decentralized agency of the European Union (EU) whose goal is to promote and protect human and animal...

ESMP enables information exchange for prevention, identification, and management of shortages to ensure medicines are available for patients in the EU and EEA. Create and manage your EMA account. Instructions on how to navigate ESMP for the purpose of shortage reporting.