We use some essential cookies to make this website work.
We’d like to set additional cookies to understand how you use GOV.UK, remember your settings and improve government services.
We also use cookies set by other sites to help us deliver content from their services.
You have accepted additional cookies. You can change your cookie settings at any time.
You have rejected additional cookies. You can change your cookie settings at any time.
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
The MSA is a unit of the Defence Logistics Organisation responsible for the provision of medical, dental and veterinary supplies to the Armed Forces.
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.
Information on the measures in the Health Service Medical Supplies (Costs) Bill.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Information and guidance on a range of medical devices for users and patients.
Order a certificate of free sale to export medical devices outside the UK.
Find out when it's possible to get zero-rated supplies on medical and research goods and services that have been funded by charities.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
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 about the EU Regulations and their implementation in Northern Ireland
How to conform with the legal requirements for placing medical devices on the market.
This paper analyses strengths and weaknesses of the public and private supply chains into the health sector
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.
You can claim relief to pay no Customs Duty or VAT if you’re importing donated medical equipment from outside the UK and EU.
Medicines and Healthcare products Regulatory Agency (MHRA) guidance on using medical devices safely.
UK guidance on re-manufacturing of Single-use medical devices.
Guidance for healthcare professionals on managing specific medicines and medical devices and using them safely.
Don’t include personal or financial information like your National Insurance number or credit card details.
To help us improve GOV.UK, we’d like to know more about your visit today. We’ll send you a link to a feedback form. It will take only 2 minutes to fill in. Don’t worry we won’t send you spam or share your email address with anyone.