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Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
Guidance for veterinary medicines manufacturers and wholesale dealers in GB on selling and supplying products placed on the EU and UK markets before 1 January 2021 and the evidence you may need to provide.
Information on comparator products used in studies supporting abridged marketing authorisation application.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
Guidance for Applicants wishing to apply for a Promising Innovative Medicines designation, pre-submission meeting or an EAMS Scientific Opinion.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
Become a Driver and Vehicle Standards Agency (DVSA) assessed compulsory basic training (CBT) motorcycle instructor - how to book your assessment and what it involves
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