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Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
A guide to farming risks, potential problems with public safety and how to avoid accidents
Code of practice on the effective prevention and control of infection by health service providers.
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 to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Controlled work application forms: representation - CW1&2 (MH), enhanced rates - CWC (MH), review of refusal or withdrawal - CW4 (MH).
How to use a cost effectiveness analysis to evaluate your digital health product.
Advice and guidance for healthcare practitioners on the health needs of migrant patients.
Facts, resources and information on major public health issues for public health professionals, local authorities and CCG commissioners.
Guidance for manufacturers on the regulations that apply to prosthetic, orthotic and ophthalmic devices.
Accidents, health and safety law and workplace conditions
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Find out about the ways people can make certain decisions for you or do certain things on your behalf
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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