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Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
What blood establishments, blood banks and manufacturers of blood products need to do to ensure the safety and quality of blood and blood products.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
How to use a cost utility analysis to evaluate your digital health product.
Information on the core components of the UK’s NQI, its four main institutions, and its role in the UK economy.
A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
How a marketing authorisation holder should report a defect with a veterinary medicine.
UK guideline on GMP for decentralised manufacturing, ensuring compliance with EU GMP principles for safe, quality medicinal products.
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