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UK MHRA Guidance: Use of Non-OECD MAD Non-Clinical Data in Support of UK Clinical Trial Authorisation
The Medicines and Healthcare products Regulatory Agency (MHRA) has published guidance on using non-clinical data generated outside the Organisation for Economic Co-operation and Development (OECD) Mutual Acceptance of Data (MAD) framework to support UK Clinical Trial Authorisation (CTA) applications. OECD MAD (Mutual Acceptance of Data) is an international agreement under which participating countries accept data generated in accordance with OECD Test Guidelines and OECD Prin
Sharan Murugan
1 hour ago4 min read