Annex 21 of EU GMP Guide – Importation of Medicinal Products – Final Version Published Annex 21 of EU GMP Guide – Importation of Medicinal Products – Final Version Published The European Commission has published... Annex 21 of EU GMP Guide – Importation of Medicinal Products – Final Version Published
EU Common Standard for Electronic Product Information – Adopted EU Common Standard for Electronic Product Information – Adopted The European Medicines Regulatory Network, following a public consultation, has adopted... EU Common Standard for Electronic Product Information – Adopted
Revision of the EU General Pharmaceuticals Legislation – Update Revision of the EU General Pharmaceuticals Legislation – Update The European Commission has published the outcome of the... Revision of the EU General Pharmaceuticals Legislation – Update
HMA 106th Meeting Highlights – November 2021 HMA 106th Meeting Highlights – November 2021 The Heads of Medicines Agencies (HMA) has published the highlights from their 106th... HMA 106th Meeting Highlights – November 2021
Digital Application Dataset Integration (DADI) Network Project Q&A Updated Digital Application Dataset Integration (DADI) Network Project Q&A Updated The European Medicines Agency (EMA) has published the updated Q&A on... Digital Application Dataset Integration (DADI) Network Project Q&A Updated
Big Data Highlights – EMA-HMA Big Data Steering Group Big Data Highlights – EMA-HMA Big Data Steering Group The first issue of the Big Data Highlights, which reports on... Big Data Highlights – EMA-HMA Big Data Steering Group
EMA HMPC Launches Calls for Submission of Scientific Data EMA HMPC Calls for Scientific Data EMA HMPC has launched calls for submission of scientific data for:... EMA HMPC Launches Calls for Submission of Scientific Data
MHRA Publishes Marketing Authorisations Granted in January 2022 MHRA’s list of marketing authorisations granted in January 2022 MHRA granted four OTC licences in January 2022. Details of these... MHRA Publishes Marketing Authorisations Granted in January 2022
MHRA Webinar – E-cigarette Submission Portal-2022 Updates, Requirements and Guidance MHRA Webinar – E-cigarette Submission Portal-2022 Updates, Requirements and Guidance Date/Time: Thursday 31 March 2022, 14:00-16:00The MHRA is hosting a... MHRA Webinar – E-cigarette Submission Portal-2022 Updates, Requirements and Guidance
MHRA Public Assessment Report – Reclassification of Buscopan IBS Relief, Hyoscine Butylbromide 10mg Tablets MHRA Public Assessment Report – Reclassification of Buscopan IBS Relief, Hyoscine Butylbromide 10mg Tablets MHRA has published the Public Assessment... MHRA Public Assessment Report – Reclassification of Buscopan IBS Relief, Hyoscine Butylbromide 10mg Tablets
EMA Webinars – Digital Application Dataset Integration Network Project – Slides and Recording EMA Webinars – Digital Application Dataset Integration Network Project Slides and Recording The European Medicines Agency (EMA) hosted a webinar... EMA Webinars – Digital Application Dataset Integration Network Project – Slides and Recording
CMDh Workplan to 2025 – Public Consultation CMDh Workplan to 2025 – Public Consultation The Co-ordination group for Mutual recognition and Decentralised procedures – human (CMDh) has published... CMDh Workplan to 2025 – Public Consultation
