安裝中文字典英文字典辭典工具!
安裝中文字典英文字典辭典工具!
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- European Medicines Agency (EMA)
The European Medicines Agency is a decentralised agency of the European Union responsible for the evaluation, supervision and safety monitoring of medicines
- EudraCT Public website - Home page
Welcome to the EudraCT public home page EudraCT (European Union Drug Regulating Authorities Clinical Trials Database) is the database for all interventional clinical trials on medicinal products that were conducted in the European Union (EU) European Economic Area (EEA) between 1 May 2004 and 30 January 2025 under Directive 2001 20 EC, as well as for all trials conducted outside of the EEA
- Login - Help - Europa
SPOR, Eudralink, EudraCT Secure, service desk portal, European union telematics controlled terms (EUTCT), meeting management system (MMSe), managing meeting document system (MMD), EudraVigilance data analysis system (EVDAS), EudraPORTAL, European Union good manufacturing and distribution practices database (EUDRAGMDP), paediatrics records application (PedRA), SIAMED business intelligence
- Eudra GMP - Public Layout - Europa
Welcome to EudraGMDP EudraGMDP is the name for the Union database referred to in article 111(6) of Directive 2001 83 EC as amended, and article 91 of Regulation (EU) 2019 6
- In-use stability testing of human medicinal products . . .
European Medicines Agency Domenico Scarlattilaan 6 1083 HS Amsterdam The Netherlands Tel: +31 (0)88 781 6000 How to find us Postal address and deliveries
- Home · EMA Account Management - Europa
Please, make sure you are using your email address to login Starting from the 8th of May 2025 EMA has deprecated access with userId with suffix "@id ema europa eu" More information on how to login to EMA systems can be found here
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