Mind the gap - connected by quality. 4th - 6th November 2026, London.
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More informationMORE Registrations - A step-by-step guide on using the MORE Platform for Registrations for Submissions of device related incidents.
Mental health funding of £1.8m welcomed by MHRA and NICE to explore regulation of digital mental health tools
Software and AI as a Medical Device Change Programme
Unique opportunity for healthcare professionals to influence future MHRA safety communications and safety reporting systems
The minutes of the ministerial annual accountability review of the Medicines and Healthcare products Regulatory Agency (MHRA).
Quarterly Summary Reports added to Medical Device Guidance
MHRA have added an 'Advertising and Promotion' Section added to NIMAR
MHRA appoints first new UK Approved Body to certify medical devices since Brexit
The European Commission (EC) have adopted the revised Annex VI to Regulation (EU) No 536/2014 (Clinical Trials Regulation, CTR)
EMA - Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 12-15 September 2022