3 July 2023 National Requirements for the Local Person for Pharmacovigilance (LPPV) in the EU, UK and Switzerland
22 June 2023 Simplified reporting procedures for monitoring the safety of clinical trials: simplified procedures for sponsors
13 June 2023 Webinar – Requirements for a local contact person for pharmacovigilance: where do you need one?
New recommendations to strengthen supply chains of critical medicines By EMA – News and press releases
Table of decisions of labelling exemption requests falling under article 63 of Directive 2001/83/EC examined by the Quality Review of Documents (QRD) Group By EMA – Regulatory and procedural guidelines
Paediatric Committee (PDCO): 23-26 April 2024, Online, European Medicines Agency, Amsterdam, the Netherlands, from 23 April 2024 to 26 April 2024 By EMA – Events
Information and Q&A session on updated CAPs in web-based eAF, Online, European Medicines Agency, Amsterdam, the Netherlands, from 7 May 2024, 10:00 (CEST) to 7 May 2024, 11:00 (CEST) By EMA – Events
Clinical Trials Information System (CTIS) Bitesize Talk: How to submit a transitional trial in CTIS, Online, Broadcast, from 29 February 2024, 16:30 (CET) to 29 February 2024, 18:00 (CET) By EMA – Events
Meeting of the Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG) – April 2024, Online, European Medicines Agency, Amsterdam, the Netherlands, from 23 April 2024, 09:00 (CEST) to 23 April 2024, 10:00 (CEST) By EMA – Events