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Register to vote Register by 18 June to vote in the General Election on 4 July.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives.
What you need to do to supply investigational medicinal products (IMPs) from Great Britain to Northern Ireland.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Chief Medical Officer for England, Professor Chris Whitty's annual reports and lectures on medicine and public health.
Importing investigational medicinal products for use in clinical trials
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Apply for a promising innovative medicine (PIM) designation or scientific opinion for your medicine from MHRA.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
The legal text underpinning the regulation of manufacture, authorisation, marketing, distribution, use and post-authorisation surveillance of veterinary medicines and medicated feed.
How to get a marketing authorisation for an Advanced Therapy Medicinal Product (ATMP) so it can be sold and/or supplied in Great Britain.
Explanation of what Pharmacovigilance means and who is responsible. These documents must be read with the Implementation Explainer at VMD Information Hub.
Links to EU guidance, as it stood immediately before end of transition period.
The mycology reference laboratory provides laboratory services for the diagnosis and management of fungal infections.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
Requirements for an Animal Test Certificate (ATC) to carry out the field trial of a veterinary medicine in animals (clinical trial) in the UK.
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