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A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
How to use an interrupted time series to evaluate your digital health product.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
List of words and phrases that will cause a veterinary product to be medicinal by presentation either through use or contextual use.
How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Clarification for the interpretation of the new elements within the Veterinary Medicines Regulations (VMRs), as amended, relating to combating antimicrobial resistance (AMR).
Comply with good pharmacovigilance practice and prepare for an inspection.
How to confirm a measles diagnosis, manage cases and contacts, control infection, and vaccinate young or partially-covered patients.
What qualifies as ordinary commuting and private travel for tax purposes.
Any person or organisation involved in a transaction with those subject to financial sanctions will first need a licence from OFSI.
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