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There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
List of manufacturers and their medical devices granted an exemption by MHRA. The list also includes manufacturers whose exemption expired or was cancelled.
How the Certification Officer (CO) applies her powers to act without a complaint to conduct investigations into trade unions and employers’ associations.
Guidance on managing and using bed rails safely.
Information and guidance on a range of medical devices for users and patients.
Order a certificate of free sale to export medical devices outside the UK.
If you put EEE on the UK market you must follow rules on both the EEE you sell and the EEE that becomes waste (WEEE).
Resources to support exams officers in their important role, covering GCSE, A level, T Level and vocational and technical qualification (VTQ) assessments
Information on MHRA's enforcement duties and how to report a non-compliant medical device.
Pharmacovigilance administrator vacancy working Pharmacovigilance section of the Authorisation Division.
The MDP uses Project Servator to disrupt criminal activity, while providing a reassuring presence for the Defence community and public.
Find out about the Industry Security Assurance Centre (ISAC) and its associated responsibilities.
Guidance on defining intended purpose for Software as a Medical Device (SaMD), to help SaMD manufacturers in meeting their statutory obligations.
How a manufacturer can apply for approval to supply a non-compliant medical device on humanitarian grounds.
Guidance for healthcare professionals covers the use, management and safety of in vitro diagnostic (IVD) devices, including blood glucose meters.
Check the legal requirements you need to meet before you can place a medical device on the market and see how MHRA monitors compliance.
The MHRA welcomes the publication of Dame Margaret Whitehead’s Equity in Medical Devices: Independent Review
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