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Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
How to use a cost utility analysis to evaluate your digital health product.
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Mental health support and advice facilities for service personnel, reservists, veterans and service families.
Advice for medical professionals to use when assessing drivers with cardiovascular disorders.
How DHSC resolves disputes in health and social care when 2 or more local authorities cannot agree responsibility for meeting a person's eligible needs.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Information about the EU Regulations and their implementation in Northern Ireland
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Guidance for commissioners and health professionals to make decisions about mental health services and interventions based on data and analysis.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
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.
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.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Tax and reporting rules for employers providing medical or dental treatment and insurance
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.
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