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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.
The MHRA will review applications for orphan designation at the time of a marketing authorisation (MA) or variation application.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
Information for patients, healthcare professionals and developers of new medicines
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
How to get a marketing authorisation for an Advanced Therapy Medicinal Product (ATMP) so it can be sold and/or supplied in Great Britain.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Apply for a promising innovative medicine (PIM) designation or scientific opinion for your medicine from MHRA.
A form of IP that extends the protection of patented active ingredients present in pharmaceutical or plant protection products.
Information about the EU Regulations and their implementation in Northern Ireland
The use of ionising radiation in medicine, including recommended dose measurements and guidance on safe radiology practice.
Find out when it's possible to get zero-rated supplies on medical and research goods and services that have been funded by charities.
Business potential of producing crops for non-food markets, how and where to grow them and details of organisations providing grants.
Information on herbal medicines, how to apply for a traditional herbal registration (THR), banned or restricted herbal ingredients, homeopathic medicines and fees.
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