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
How to create a model of how your digital health product works and choose measures for your evaluation.
How to use a quasi-experimental study to evaluate your digital health product.
List of business critical models that support MOD policy, in response to the Macpherson review of quality assurance of analytical models.
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.
Guidance for suppliers and dealers.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
These documents cover the detail of Public Health England’s (PHE) review of the Nutrient Profiling Model (NPM).
Get help to classify plastics for import and export.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to move groups of agrifood products from Great Britain to Northern Ireland and how to prepare your consignment for checks at the point of entry.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Types of model articles of association a limited company can have, including older versions of Table A from previous company legislation.
How to use a before-and-after study to evaluate your digital health product.
How to use an interrupted time series to evaluate your digital health product.
Tools and guidance to help people Quality Assure (QA) new and existing energy security and net zero models, including those developed by third parties.
How to import animals and animal products to Great Britain (England, Scotland and Wales), the Channel Islands and the Isle of Man from non-EU countries.
Find out which standards and regulations apply to your product and how to make sure you follow the right procedures.
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.