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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 a manufacturer can apply for approval to supply a non-compliant medical device on humanitarian grounds.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Guidance for commissioners and health professionals to make decisions about mental health services and interventions based on data and analysis.
Information about incidents and outbreaks of Ebola and Marburg, both viral haemorrhagic fevers (VHF).
There are changes to the legislation of Reference Medicinal Products (RMPs) used to support abridged marketing authorisation applications
How we engage and involve patients and the public in our regulatory decision-making.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
How to apply for repayment of import duty and VAT on protective equipment or medical supplies brought into the UK from non-EU countries from 30 January 2020 up to 31 December 2020.
How to get fast-track approval of medical devices during COVID-19.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Using an ecological momentary assessment to evaluate your digital health product.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to use a cost utility analysis to evaluate your digital health product.
How to get state healthcare if you live, work or study in Belgium.
List of medical repatriation companies for British nationals who are seriously ill or injured abroad and need medical evacuation to the UK.
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