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Explains what quality assurance is and the processes involved.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
The MHRA has today set out its strategic approach to artificial intelligence (AI)
Guidance for hospitals, tissue establishments and fertility clinics for ensuring the quality and safety of human organs, tissues and cells (including reproductive cells).
Information about the EU Regulations and their implementation in Northern Ireland
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
Information and guidance on a range of medical devices for users and patients.
This document details the service standards of the Veterinary Medicines Directorate (VMD)
A summary of what delivering better integrated care means and how Monitor is supporting the sector.
Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
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