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Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How the MHRA makes decisions on what is a medicinal product (borderline products).
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
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