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
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
This guidance explains the different preference tiers under the DCTS, including benefits for each tier, criteria for moving between tiers and transition periods.
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
How to apply for a traditional herbal registration (THR) to market a herbal medicine in the UK.
You can become a DVSA enhanced rider scheme trainer if you want to train fully qualified motorcyclists in the scheme
This series brings together all documents relating to Guidance and methods
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
How to use an interrupted time series to evaluate your digital health product.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Oct - 31 Dec 2023.
Check the tariff classification for peptide nisin standardised with sodium chloride
Check and improve your motorcycle riding skills with an enhanced rider scheme trainer
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
The Fund aims to create the opportunity to build strong partnerships between UK and Turkish scientists, researchers and institutions.
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
A strategy for education providers and the technology industry to help improve and increase the effective use of technology in education.
Information for British nationals affected by rape or sexual assault abroad, including how to access medical treatment and legal advice in the UK.
This amended guidance was issued under s 182 of the Licensing Act 2003.
Dose of nicotine delivered & uptake and consistency of dose.
How to get accredited so your laboratory can perform official paternity tests as instructed by a court.
How the MHRA makes decisions on what is a medicinal product (borderline products).
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.