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
Register to vote Register by 18 June to vote in the General Election on 4 July.
Did you mean Falsified medicines
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
Medicines that were granted a positive opinion under the early access to medicines scheme (EAMS) which has now expired.
Further documents relating to the Medicines and Medical Devices Bill 2020.
To help you protect, manage and enforce your intellectual property (IP) rights in Philippines.
Information on MHRA's enforcement duties and how to report a non-compliant medical device.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices and a reminder of a recent MHRA National Patient Safety Alert to highlight the potential risk of underdosing with calcium gluconate in severe hyperkalaemia....
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
Legal requirements for the sale of veterinary medicines on the internet and the VMD Accredited Internet Retailer Scheme (AIRS).
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Advice for medical professionals to follow when assessing drivers with drug or alcohol misuse or dependence.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
How to conform with the legal requirements for placing medical devices on the market.
The legal text underpinning the regulation of manufacture, authorisation, marketing, distribution, use and post-authorisation surveillance of veterinary medicines and medicated feed.
The CMA investigated the anticipated acquisition by Cochlear Limited of the hearing implants business of Demant A/S, known as Oticon Medical.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
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. Please fill in this survey (opens in a new tab).