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Homepage | European Medicines Agency. Safety committee meeting: July 2024 highlights. New recommendation to minimise risk of aspiration with GLP-1 medicines during anaesthesia. Read highlights. EU actions to tackle shortages of GLP-1 receptor agonists. New recommendations to ensure these medicines reach those who need them most.
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 a decentralised agency of the European Union (EU) responsible for the scientific evaluation, supervision and safety monitoring of medicines in the EU.
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). What it does. The Agency's main responsibilities are authorising and monitoring medicines in the EU.
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 ).
Jul 16, 2024 · All Marketing Authorisation Holders (MAHs) product contact points should ensure they are registered in the EMA Account Management System by October 2024. This is part of the transition of all EMA-led post-authorisation procedures to IRIS planned for January 2025.
The HMA-EMA Catalogues are repositories of metadata collected from real-world data (RWD) sources and RWD studies. They are intended to help regulators, pharmaceutical companies and researchers to identify and use such data when investigating the use, safety and effectiveness of medicines.
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. EMA Working for every patient in Europe (video in English, with subtitles in 24 different languages) ~ 2 mins.
Jun 5, 2024 · Energy Market Authority (EMA) is the government agency that drives the advancement of Singapore's energy future that is resilient, sustainable and competitive.
Jun 6, 2024 · EMA is the first regulatory authority worldwide to provide such broad access to clinical data. For more information on the clinical data on this website, see Clinical data available. For more information on EMA and its policy on the publication of clinical data, see the EMA corporate website.
