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Medicinal products - Latest updates (315)
RSS![2023 Pharma strategy](https://health.ec.europa.eu/sites/default/files/styles/oe_theme_ratio_3_2_medium/public/2023-04/mp_20230426_spotlight.jpg?itok=bMG7fWbp)
European Health Union: Commission proposes pharmaceuticals reform for
more accessible, affordable and innovative medicines
Questions and Answers on the pharmaceutical legislation
Questions and Answers on the Recommendation on Antimicrobial Resistance
Quick guide for sponsors - Regulation 536/2014 in practice (Eudralex vol. 10)
Presentations and video recordings - Multistakeholder Event on Biosimilar medicines (13 December 2022)
Improving the quality of medicines
Clinical Trials: EU survey on the implementation of the Clinical Trial Regulation
Agenda and Pre-registration - Webinar on Best practices in the public procurement of medicines (7 February 2023, 10:00-12:30 CET)
EU Guideline on orphan applications (for designation and transfer) - 2022/C 440/02
Recommendation paper on decentralised elements in clinical trials
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Pharmaceuticals: Commission proposes updated EMA fees
Biosimilar medicines - Multistakeholder Event (13 December 2022)
Staff Working Document on Vulnerabilities of the global supply chains of medicines – Structured Dialogue on the security of medicines supply
Agenda - 100th meeting of the Pharmaceutical Committee (21 October 2022)
Civil Society representatives: Call for expressions of interest for the EMA PDCO Committee
Update - EudraLex - Volume 10 - Clinical trials guidelines - Questions and Answers Document - Regulation (EU) 536/2014 – Version 6.2 (September 2022)
Revision - Manufacture of Sterile Medicinal Products
Summary record - 99th meeting of the Pharmaceutical Committee (11 May 2022)
Questions and answers - Complex clinical trials
Questions and Answers Document – Regulation (EU) 536/2014 – Version 6.1, May 2022