The European Medicines Agency recently launched a public consultation on a draft Concept paper on Good Manufacturing Practice and Marketing Authorisation Holders. EIPG has reviewed the document and, following feedback from its members, has submitted its comments to the EMA.
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News from EIPG
- Annex 1 – a focus on its main issues (Webinar)
- How a pandemic has affected the pharma industry (Webinar)
- EIPG publishes updated version of Code of Practice for Qualified Persons
- Consultation on Annex 21: Importation of medicinal products, of the EudraLex Volume 4 (Webinar)
- The role of the body clock in drug development, efficacy and toxicity (Webinar)
- Medicines shortages: root causes and potential solutions
- GMP documentation management: requirements and best practices (Webinar)
