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
Checklists providing a practical guide to using medical devices.
Update on MHRA UK risk-based GxP inspection programme.
Guidance for industry on preparing responses to good laboratory practice (GLP) and good clinical practice (GCP) inspection reports.
summary
Guidance for industry on flexible approaches we are taking on good distribution practices.
Ten guiding principles that can inform the development of Good Machine Learning Practice (GMLP).
The review of the safety of isotretinoin has concluded.
What 'single-use' means and what symbol is used by manufacturers to show this.
Guidance and specifications for the recording and extraction of CTAD data from laboratories in England processing LA and NHS commissioned chlamydia tests.
This external quality assessment (EQA) scheme is suitable for laboratories that routinely test for a range of food-borne pathogens and indicator organisms.
Guidance for manufacturers on the regulations that apply to prosthetic, orthotic and ophthalmic devices.
Protocol, questionnaire and quarterly return form for the enhanced surveillance of post-herpetic neuralgia (PHN), a complication of shingles.
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
Guidance on moving medicines by air
We are allowing alternative courses of actions for manufacturing or laboratory equipment during the outbreak.
Data submission requirements for acute, community and private microbiology services submitting data on all LA/NHS chlamydia tests done in England.
Poster with advice for healthcare professionals on how to carry out point of care testing safely and correctly.
Qualified Persons (QPs) should follow the below guidance on the flexible approaches we are taking for medicines imported from third countries.
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).