New Commissioners Appointed to the Commission on Human Medicines New Commissioners Appointed to the Commission on Human Medicines Professor Tony Williams, Professor David Hunt, Professor David Dockrell, Dr Gerri... New Commissioners Appointed to the Commission on Human Medicines
Big Data – HMA-EMA Joint Big Data Taskforce Workplan Update: 2022-2025 Big Data – HMA-EMA Joint Big Data Taskforce Workplan Update: 2022-2025 The Big Data Steering Group set... Big Data – HMA-EMA Joint Big Data Taskforce Workplan Update: 2022-2025
EU Pharma Legislation Review – Proposed Amendments to Directive 2001/83 EU Pharma Legislation Review – Proposed Amendments to Directive 2001/83 AESGP are working with EFPIA and Medicines for Europe on... EU Pharma Legislation Review – Proposed Amendments to Directive 2001/83
EMA Guideline on the Chemistry of Active Substances – Public Consultation EMA Guideline on the Chemistry of Active Substances – Public Consultation The EMA (European Medicines Agency) has published the... EMA Guideline on the Chemistry of Active Substances – Public Consultation
EMA Q&A and Report Published on Boric Acid and Borates used as Excipients in Human Medicines EMA Q&A and Report Published on Boric Acid and Borates used as Excipients in Human Medicines Further to the European... EMA Q&A and Report Published on Boric Acid and Borates used as Excipients in Human Medicines
Fourth Watch List of Substances Published in Official Journal Fourth Watch List of Substances Published in Official Journal The Commission Implementing Decision (EU) 2022/1307 of 22 July 2022 establishing... Fourth Watch List of Substances Published in Official Journal
One Substance One Assessment – Commission Consultation One Substance One Assessment – Commission Consultation The European Commission has launched a second call for evidence concerning a possible... One Substance One Assessment – Commission Consultation
DHSC Guidance – Reporting Requirements for Medicine Shortages and Discontinuations Updated DHSC Reporting Requirements for Medicine Shortages and Discontinuations The Department of Health and Social Care (DHSC) has updated their guidance... DHSC Guidance – Reporting Requirements for Medicine Shortages and Discontinuations Updated
EU IDMP Implementation Guide v 2.1.1 Released EU IDMP Implementation Guide v 2.1.1 Released The European Medicines Agency (EMA) has released the updated version of the... EU IDMP Implementation Guide v 2.1.1 Released
PAGB Consultation Response – The Future Strategy for Batch Testing of Medicinal Products in Great Britain PAGB Consultation Response – The Future Strategy for Batch Testing of Medicinal Products in Great Britain The Department of Health... PAGB Consultation Response – The Future Strategy for Batch Testing of Medicinal Products in Great Britain
Updated Annex to EC Guideline on Excipients in Labelling & Package Leaflet – Update on Boric Acid Updated Annex to EC Guideline on Excipients in Labelling & Package Leaflet – Update on Boric Acid The European Medicines... Updated Annex to EC Guideline on Excipients in Labelling & Package Leaflet – Update on Boric Acid
MHRA Publishes 2021 Annual Report of the Human Medicines Regulations 2012 Advisory Bodies MHRA Publishes 2021 Annual Report of the Human Medicines Regulations 2012 Advisory Bodies The Medicines and Healthcare product Regulatory Agency... MHRA Publishes 2021 Annual Report of the Human Medicines Regulations 2012 Advisory Bodies
