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Information to support your recovery after COVID-19.
Find out about the long-term effects some people can have after having COVID-19.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Employment Appeal Tribunal Judgment on Recusal Application of Judge Tayler on 30 April 2024.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Using an ecological momentary assessment to evaluate your digital health product.
How to use an interrupted time series to evaluate your digital health product.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Find out about applications to protect traditional terms related to wine products in Great Britain.
What Works to Prevent Violence against Women and Girls: funding opportunity. Aims to build knowledge on what works to prevent violence against women and girls (VAWG).
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Foreign, Commonwealth & Development Office (FCDO) advice for lesbian, gay, bisexual and transgender (LGBT+) people travelling abroad.
Guidance for the pharmaceutical industry on who can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
Find UK trade data from HMRC. Look up data about imports, exports, commodities and traders.
How to use a crossover randomised controlled trial to evaluate your digital health product.
How to use a before-and-after study to evaluate your digital health product.
Free and impartial help with money and pensions.
How to get a parallel import licence for your medicine in the UK, including pharmacovigilance requirements and submitting your application.
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