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How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Safety leaflet on topical corticosteroids and withdrawal reactions to help patients and their carers to use these medicines safely.
The CMA investigated alleged excessive and unfair pricing, anti-competitive agreements and abusive conduct with respect to hydrocortisone tablets under Chapters I and II CA98 and Articles 101 and 102 TFEU.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
NHS Business Services Authority contact number for ordering prepaid prescriptions for 3 or 12 months at a cheaper rate than single prescriptions
AnimalBiome product seized at East Midlands Airport.
How the MHRA makes decisions on what is a medicinal product (borderline products).
How to use a crossover randomised controlled trial to evaluate your digital health product.
A form of IP that extends the protection of patented active ingredients present in pharmaceutical or plant protection products.
How to use a quasi-experimental study to evaluate your digital health product.
Use this form to supplement your application for a search warrant or production order under Police and Criminal Evidence Act 1984, and the Crime (International Co-operation) Act 2003, section 16.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Reported problems with the supply of an animal medicine and the date when the issue is expected to be resolved.
How to complete supplementary pages CT600H and what information you need to include.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How to complete supplementary pages CT600L and what information you need to include.
Urgent safety updates arising from pharmacovigilance data, including reported adverse events, for veterinary medicines authorised in the UK.
This amended guidance was issued under s 182 of the Licensing Act 2003.
Use this form to provide additional information when you are making an application for a warrant to assist a person authorised by an emergency protection order.
Don’t include personal or financial information like your National Insurance number or credit card details.
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