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An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Look up a trade mark to see if something identical or similar to your brand is already registered.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
The MHRA is part of the Access Consortium along with the Therapeutic Goods Administration, Health Canada, Health Sciences Authority of Singapore and Swissmedic.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
How to use A/B testing to evaluate your digital health product.
Check the patents journal to find UK-registered patents granted, published and filed
How to get fast-track approval of medical devices during COVID-19.
Background information and advice on coronavirus (COVID-19) for health and care professionals.
Volume 31 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Coronavirus (COVID-19) vaccination consent form and letter templates for healthcare workers.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Apply for a promising innovative medicine (PIM) designation or scientific opinion for your medicine from MHRA.
Find out about tax charges on scholarships.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
Countries have their own rules about what goods you can bring in using an ATA Carnet. Check with the issuer in the country you’re exporting to.
News and guidance on veterinary medicines issues affected by coronavirus (COVID-19).
This guidance identifies common issues with validation and assessment of clinical trial applications and how to avoid them.
Don’t include personal or financial information like your National Insurance number or credit card details.
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