MDR Implementation – Speech by Commissioner Kyriakides on the Revision of MDR MDR Implementation – Speech by Commissioner Kyriakides on the Revision of MDR On 24 November, Health Commissioner Stella Kyriakides gave... MDR Implementation – Speech by Commissioner Kyriakides on the Revision of MDR
MHRA Good Manufacturing and Distribution Practice Symposia 2023 MHRA Good Manufacturing and Distribution Practice Symposia 2023 Between 21 February – 22 February 2023 MHRA is hosting the Good... MHRA Good Manufacturing and Distribution Practice Symposia 2023
Revisions of MDCG Guidance Documents on Safety Reporting in Clinical Investigations Published Revisions of MDCG Guidance Documents on Safety Reporting in Clinical Investigations Published The Commission has published a revised version of... Revisions of MDCG Guidance Documents on Safety Reporting in Clinical Investigations Published
MHRA Guidance on Borderline Products Updated MHRA Guidance on Borderline Products Updated The MHRA has updated their guidance ‘Borderline products: how to tell if your product... MHRA Guidance on Borderline Products Updated
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
