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Data, Freedom of Information releases and corporate reports
The Wellcome Trust has funded a 3-year project focusing on effective regulation and evaluation of digital mental health technology.
Information about the EU Regulations and their implementation in Northern Ireland
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Information for prospective growers of low THC cannabis (industrial hemp), for the production of seed and fibre only.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
The MHRA has authorised cabotegravir as 30 mg tablets and as a 600 mg long-acting injection administered every two months
Order a certificate of free sale to export medical devices outside the UK.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
How to conform with the legal requirements for placing medical devices on the market.
The government's response to the Health and Social Care Committee's report.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
Information and guidance on a range of medical devices for users and patients.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
List of manufacturers and their medical devices granted an exemption by MHRA. The list also includes manufacturers whose exemption expired or was cancelled.
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