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Register to vote Register by 18 June to vote in the General Election on 4 July.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Apply for a promising innovative medicine (PIM) designation or scientific opinion for your medicine from MHRA.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
This guidance demonstrates stakeholders, including the government, working together to address supply issues.
Guidance for industry on flexible approaches we are taking on good distribution practices.
Information for patients, healthcare professionals and developers of new medicines
Apply for an import certificate to import a medicinal product into the UK for veterinary use.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
How veterinary medicines can be advertised.
Guidance for prescribing vets on the use of the cascade.
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How the MHRA makes decisions on what is a medicinal product (borderline products).
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
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