Mhra Medical Device Contacts

Contact MHRA - GOV.UK

https://www.gov.uk/guidance/contact-mhra

MHRA medicines portal Regulatory information service (RIS) Whistleblower referrals Distance Selling Logo Data protection Print this page Customer Services 10 South Colonnade Canary Wharf London...

Register medical devices to place on the market - GOV.UK

https://www.gov.uk/guidance/register-medical-devices-to-place-on-the-market

Please contact the MHRA by emailing [email protected] for advice on how to register your custom-made devices if: you are a manufacturer …

Regulating medical devices in the UK - GOV.UK

https://www.gov.uk/guidance/regulating-medical-devices-in-the-uk

Medicines and Healthcare products Regulatory Agency

https://www.gov.uk/government/organisations/medicines-and-healthcare-products-regulatory-agency

MHRA 10 South Colonnade London E14 4PU United Kingdom Email [email protected] Telephone 020 3080 6000 Fax 020 3118 9803 Office hours are Monday to Friday, 9am to …

Medical devices: guidance for manufacturers on vigilance

https://www.gov.uk/government/collections/medical-devices-guidance-for-manufacturers-on-vigilance

Enter ‘UKRP’ and complete the contact details in Section 1.3.4. ‘Submitters details’. For more details on how to submit reports please refer to the guidance document …

Medical device safety information produced by the MHRA

https://www.gov.uk/drug-device-alerts/medical-device-safety-information-produced-by-the-mhra

The MHRA may directly inform specific organisation that we know have a particular device or contact organisations such as professional bodies or charities …

New UK MHRA Medical Devices Regulations Published - NAMSA

https://namsa.com/uk-mhra-medical-device-regulations-published/

New UK MHRA Medical Devices Regulations Published | NAMSA On 26 June 2022, the United Kingdom’s Medical Devices and Healthcare Regulatory Authority …

Complaints procedure - Medicines and Healthcare …

https://www.gov.uk/government/organisations/medicines-and-healthcare-products-regulatory-agency/about/complaints-procedure

The Adverse Incident Centre ( AIC) The AIC processes reports of adverse incidents involving medical devices and equipment. Email: [email protected] Telephone: 020 …

UK MHRA Updates Roadmap for New Medical Device Regulations

https://www.emergobyul.com/news/uk-mhra-updates-roadmap-new-medical-device-regulations

The MHRA highlighted patient safety and benefit, “need for patient safety and being supportive in an operating environment to support industry and patients,” …

Yellow Card | Making medicines and medical devices safer

https://yellowcard.mhra.gov.uk/?UNLID=7446211142023216235533

Use the Coronavirus Yellow Card reporting site to report suspected side effects to medicines and vaccines or medical device and diagnostic adverse incidents used in coronavirus …