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
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
Work out the VAT liability of goods and services supplied by health and care institutions and providers of non residential care to children.
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.
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).
Guide for overseas investors on how to access NHS procurement channels.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
What you need to do now that the eCommerce Directive no longer applies to the UK.
How to use a patient-reported outcomes and experiences study to evaluate your digital health product.
Eligible health and social care providers can order PPE through the portal to meet the increased need that has arisen as a result of the COVID-19 pandemic.
Guidelines for the monitoring of volume individual voluntary arrangement (IVA) and protected trust deed (PTD) providers
If you’re a business, organisation or sole trader that uses PPPs and adjuvants professionally in Great Britain, register to comply with regulations.
We’re working to help people securely prove who they are without having to rely on physical documents.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
This guidance outlines how to make informed choices about your organisation’s reliance on cloud technologies.
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).