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This guidance sets out how the MHRA is handling centralised applications that were still pending on 1 January 2021.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
How to use a quasi-experimental study to evaluate your digital health product.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
How to use a crossover randomised controlled trial to evaluate your digital health product.
How to begin with evaluating a digital health product, including when to evaluate, budgeting and getting support.
How to use a cost effectiveness analysis to evaluate your digital health product.
Dose of nicotine delivered & uptake and consistency of dose.
Submission dates and how the submissions using the EC decision reliance procedure work.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
Things to consider when buying and using products.
How product specific rules are used to identify the country of origin when importing or exporting between the UK and EU.
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
How to object to an application to register for UK geographical indication (GI) protection, change or cancel a product specification and how to appeal against a decision.
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
How a marketing authorisation holder should report a defect with a veterinary medicine.
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