Message from Mark Grumbridge
My name is Mark Grumbridge and I am a senior clinical advisor at the Medicines and Healthcare Products Regulatory Agency (MHRA).
MHRA is an executive agency of the Department of Health and Social Care in the United Kingdom which is responsible for ensuring that medicines and medical devices work and are acceptably safe. As part of our work in devices we review applications for clinical trials for medical devices. In some situations we do not have the internal expertise and are reliant on external experts to review such applications and provide an expert opinion, We also utilise our experts for ‘ad hoc’ advice on specific issues.
Currently, we do not have any experts in stoma care and are looking to recruit new experts to the register.
MHRA will pay you a fee of (£800) for a clinical trial review however, we do not make any payment for the ‘ad hoc’ advice
If you are interested in joining our register the please refer to relevant documents (see below) where you will find more information. Please return your completed documents to me for processing.
Senior Clinical Advisor
Clinical Governance and Audit Lead
Devices Clinical Team
Tel: +44 (0) 20 3080 7128
MHRA Letter ASC
RoE Contact Details Form
Confidentiality Contract - REVISED
RoE-Pre Clinical Assessors Guideance
RoE Oracle Fusion Template