MHRA Publishes Access Consortium Good Manufacturing Practice (GMP) Statement MHRA Publishes Access Consortium Good Manufacturing Practice (GMP) Statement In alignment with the Access Consortium’s strategic objective to expand and... MHRA Publishes Access Consortium Good Manufacturing Practice (GMP) Statement
MHRA Consultation on Proposals to Increase Statutory Fees – PAGB Response MHRA Consultation on Proposals to Increase Statutory Fees – PAGB Response MHRA is seeking views on proposals for changes to... MHRA Consultation on Proposals to Increase Statutory Fees – PAGB Response
EUDAMED – Production Release 2.9 Delayed EUDAMED – Production Release 2.9 Delayed EUDAMED is the IT system developed by the European Commission to... EUDAMED – Production Release 2.9 Delayed
MHRA Webinar – Changes to E-cigarettes: Regulations for Consumer Products Guidance MHRA Webinar – Changes to E-cigarettes: Regulations for Consumer Products Guidance MHRA has updated its E-cigarettes: Regulations for Consumer Products... MHRA Webinar – Changes to E-cigarettes: Regulations for Consumer Products Guidance
MHRA Webinar Recording – Changes to the Submission Routes for Reporting Medical Device Adverse Incidents MHRA Webinar Recording – Changes to the Submission Routes for Reporting Medical Device Adverse Incidents On Tuesday 4 October 2022... MHRA Webinar Recording – Changes to the Submission Routes for Reporting Medical Device Adverse Incidents
MHRA Guidance on Pharmacovigilance Procedures Updated MHRA Guidance on Pharmacovigilance Procedures Updated The MHRA has updated their guidance on Pharmacovigilance Procedures which summarises MHRA’s approach to... MHRA Guidance on Pharmacovigilance Procedures Updated
MHRA Board Meeting – 15 November 2022 MHRA (Medicines and Healthcare products Regulatory Agency) Board Meeting – 15 November 2022 The MHRA Board will meet in public... MHRA Board Meeting – 15 November 2022
MDCG Guidance on Authorised Representatives Published MDCG Guidance on Authorised Representatives Published The Commission has published on its website the final Medical Device Coordination Group (MDCG)... MDCG Guidance on Authorised Representatives Published
MHRA Delivery Plan 2021-2023 – Updates for Year Two MHRA Delivery Plan 2021-2023 – Updates for Year Two The Delivery Plan 2021-2023 ‘Putting patients first; A... MHRA Delivery Plan 2021-2023 – Updates for Year Two
MHRA September Board Meeting Documents MHRA September Board Meeting Documents The agenda and board papers from the MHRA board meeting on 20... MHRA September Board Meeting Documents
MDCG Q&A Requirements Relating to Notified Bodies – Updated MDCG Q&A Requirements Relating to Notified Bodies – Updated An updated version (version 4) of the MDCG ‘Questions and answers:... MDCG Q&A Requirements Relating to Notified Bodies – Updated
EU Commission Updates the Rolling Plan Containing List of Essential Implementing Acts for the EU MDR European Commission Updates Rolling Plan The European Commission has updated the Rolling Plan (as of October 2022)... EU Commission Updates the Rolling Plan Containing List of Essential Implementing Acts for the EU MDR
