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How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Among a cohort of hypertensive patients in South India: 3-months follow-up study
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
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.
A summary of what delivering better integrated care means and how Monitor is supporting the sector.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
Past and current clinical trials into therapeutic and antiviral treatments for COVID-19, how to take part, and which treatments have proven to be effective.
The process for the simultaneous review of veterinary medicine submissions by New Zealand’s Ministry for Primary Industries (MPI) and the UK's Veterinary Medicines Directorate.
Guidance and information on integrated care.
Project Orbis is a programme to review and approve promising cancer drugs helping patients access treatments faster.
Guidance for prescribing vets on the use of the cascade.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Reported problems with the supply of an animal medicine and the date when the issue is expected to be resolved.
How to get a parallel import licence for your medicine in the UK, including pharmacovigilance requirements and submitting your application.
The CMA acts to help NHS patients access combination therapies used to treat serious medical conditions.
The process for the simultaneous review of veterinary drug submissions by Health Canada’s Veterinary Drugs Directorate and the UK's Veterinary Medicines Directorate.
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