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Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Information and guidance on a range of medical devices for users and patients.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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.
List of manufacturers and their medical devices granted an exemption by MHRA. The list also includes manufacturers whose exemption expired or was cancelled.
FCDO travel advice for Brazil. Includes safety and security, insurance, entry requirements and legal differences.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to apply for repayment of import duty and VAT on protective equipment or medical supplies brought into the UK from non-EU countries from 30 January 2020 up to 31 December 2020.
Guidance for people with symptoms of a respiratory infection including COVID-19, or a positive test result for COVID-19.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
How the MHRA makes decisions on what is a medicinal product (borderline products).
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
How to get state healthcare when you’re on holiday or travelling to Spain.
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