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
Find out what methods you can use to process ABPs, how to test your products for bacteria and how to permanently mark high risk material.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Compare different evaluation approaches and choose an appropriate method.
How the MHRA makes decisions on what is a medicinal product (borderline products).
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
Ensuring you get what you pay for.
Find out which types of food are zero-rated and which are standard-rated for VAT purposes.
Check the tariff classification for vitamin gummies.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
How schools can share daily attendance data.
Guidance on the 150-day assessment timeline for high-quality marketing authorisation applications including information on how to apply.
How to begin with evaluating a digital health product, including when to evaluate, budgeting and getting support.
How to import plants, fruit, vegetables, cut flowers, trees, seeds and used agricultural machinery to Great Britain (England, Scotland and Wales) from the EU, Liechtenstein and Switzerland.
Find out what compound products are, and how to import or move them from the EU to Great Britain.
Resources to help anyone developing or running a digital health product to conduct an evaluation.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Animal by-products (ABPs) you can use to make pet food, how to provide samples, and how to package your products.
How to use a cost consequence analysis to evaluate your digital health product.
The process for applicants applying for a Paediatric Investigation Plan (PIP) modification or waiver.
Find out the information you must give to customers on food products and how to give it.
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.