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How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to apply for repayment of import duty and VAT on protective equipment or medical supplies brought into the UK from non-EU countries from 30 January 2020 up to 31 December 2020.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Information about the EU Regulations and their implementation in Northern Ireland
Leading food delivery companies will introduce enhanced security checks on their apps to prevent the market being abused by illegal workers, following discussions with the government.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
An MHRA and NICE partnership, funded by Wellcome, is addressing key challenges for regulating and evaluating digital mental health technologies (DMHTs) with input from patients, the public and mental health professionals.
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.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
Foreign, Commonwealth & Development Office (FCDO) advice for lesbian, gay, bisexual and transgender (LGBT+) people travelling abroad.
Information for healthcare professionals on how pulse oximeters are regulated, home use and issues to look out for when using the devices
List of manufacturers and their medical devices granted an exemption by MHRA. The list also includes manufacturers whose exemption expired or was cancelled.
Guidance for manufacturers who don’t design or manufacture devices but place their names on the product.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
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