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 account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
This research applies to low-income and middle-income countries in the Eastern Mediterranean Region
Information for healthcare professionals on how pulse oximeters are regulated, home use and issues to look out for when using the devices
Information and documents on Public Health England’s review of the evidence for dependence on, and withdrawal from, prescribed medicines.
Explains changes to drug driving law and the guidance available for healthcare professionals and users of prescription medicine.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Actions that trial sponsors should consider to build resilience into clinical trial design
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
Advice for medical professionals to follow when assessing drivers with drug or alcohol misuse or dependence.
Information about new applications, post-licensing, advertising, product information and fees.
Guidance developed jointly with 11 organisations, including the Department of Health, representing the different parts of the supply chain.
A series of indicators to inform safer prescribing practice to help pharmacists, clinicians and patients review prescribed medication and prevent harm.
How to submit your periodic safety update report report (PSUR) or periodic benefit risk evaluation report (PBRER)
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
The guidance sets out the key legal and ethical obligations that manufacturers, wholesalers, NHS Trusts, registered pharmacies and dispensing doctors have in the supply and trading of medicines. Recent increases in the export of medicines are a major contributor to...
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
You must get permission to export certain drugs and medicines.
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.