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How to get access to MHRA submissions portals, how to use them, where to go for help.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
What you need to do as a food and drink business to work with the EU.
Guidance on applying for a Marketing Authorisation for Decentralised Manufacture, including eligibility, process, and requirements.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
Check if you're affected by the Clean Heat Market Mechanism (CHMM). See what actions you must take each scheme year.
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