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UK MHRA Updates Guidance: GCP Inspections and Clinical Investigations for Medical Devices
The Medicines and Healthcare products Regulatory Agency (MHRA) has updated two guidance documents covering Good Clinical Practice (GCP) inspections for medicinal product clinical trials and clinical investigations for medical devices. Both guidance documents were updated on 6 November 2026, providing information on regulatory compliance, inspection procedures, application requirements and clinical investigation responsibilities. 1. Clinical Trials for Medicines: Good Clinical

Sharan Murugan
1 hour ago4 min read
