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Register to vote Register by 18 June to vote in the General Election on 4 July.
List of manufacturers and their medical devices granted an exemption by MHRA. The list also includes manufacturers whose exemption expired or was cancelled.
How we engage and involve patients and the public in our regulatory decision-making.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Help available and steps you should take if you have a medical emergency or are hospitalised abroad, including for planned treatment.
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
Check the legal requirements you need to meet before you can place a medical device on the market and see how MHRA monitors compliance.
How to get fast-track approval of medical devices during COVID-19.
Guidance on defining intended purpose for Software as a Medical Device (SaMD), to help SaMD manufacturers in meeting their statutory obligations.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Guidance for industry and organisations to follow from 1 January 2021.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Report a problem ('adverse incident') with a medical device or medicine to MHRA using the Yellow Card Scheme
Information about seafarer working and living rights - working conditions, conditions of employment, safe working practices, living conditions, dangerous cargo, health and medical care, maritime labour convention, human element
Get a medical certificate to work at sea - ENG 1 or ML5 medical certificates, how much they cost, how to apply.
The regulations about working in any healthcare role, and how to register with the appropriate accredited bodies.
The functions of the Board were taken over by the Health Protection Agency in 2003, which itself became part of Public Health England in 2013.
Board meeting minutes of the Trade Remedies Authority.
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