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Reports, analysis and official statistics
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Data, Freedom of Information releases and corporate reports
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
From brussels sprouts to dodgy diet products, these tips from the MHRA will help you stay safe during the festive season and beyond
Safety leaflet on opioid medicines to help patients and their families reduce the risks of harm.
Information for patients, healthcare professionals and developers of new medicines
Advice for British people with mental health needs, and their families and carers, while travelling or living abroad.
Information and guidance on a range of medical devices for users and patients.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
How the MHRA makes decisions on what is a medicinal product (borderline products).
FCDO travel advice for Colombia. Includes safety and security, insurance, entry requirements and legal differences.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
Report a problem ('adverse incident') with a medical device or medicine to MHRA using the Yellow Card Scheme
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Safety leaflet on topical corticosteroids and withdrawal reactions to help patients and their carers to use these medicines safely.
FCDO travel advice for Brazil. Includes safety and security, insurance, entry requirements and legal differences.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Foreign, Commonwealth & Development Office (FCDO) advice for lesbian, gay, bisexual and transgender (LGBT+) people travelling abroad.
Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
Detailed guidance on advertising and promoting medicines.
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
Don’t include personal or financial information like your National Insurance number or credit card details.
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