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Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
The process for applicants applying for a Paediatric Investigation Plan (PIP) modification or waiver.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Cancel a marketing authorisation, traditional herbal registration or parallel import product licence or withdraw a pending submission.
How to get plant breeders' rights and what protection it gives your plant varieties.
Sets out medicines that cannot be exported from the UK or hoarded because they are needed for UK patients.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Information relating to the disapplication of falsified medicines under UK Law.
A community of interest for academic institutions to partner with Dstl on deterrence and related topics such as assurance, coercion and conflict escalation.
Guidance on applying to renew a marketing authorisation (MA) for a veterinary medicine.
This guidance sets out how the MHRA is handling centralised applications that were still pending on 1 January 2021.
This page includes summaries of the winning bids for the Future RAN (FRANC) competition
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to access the historical censuses from 1841 to 1921.
Apply for protection against infringements of intellectual property rights on imports into and exports out of the UK.
How to apply for marketing authorisation via this new procedure.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
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