Mhra Medical Device Registration

Register medical devices to place on the …

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

Public Access Database for Medical Device Registration

https://aic.mhra.gov.uk/era/pdr.nsf/Search?openform

Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA) Where a conformity assessment certificate is listed as …

Register to make submissions to the MHRA - GOV.UK

https://www.gov.uk/guidance/register-to-make-submissions-to-the-mhra

Registering for the MHRA Gateway Once you have completed registration for MHRA Submissions, MHRA Submissions company administrators can register to …

MHRA Guidance on Registration of Medical Devices

https://www.regdesk.co/mhra-guidance-on-registration-of-medical-devices/

MHRA Guidance on Registration of Medical Devices Jun 8, 2021 The Medicines and Healthcare products Regulatory Agency (MHRA), the UK regulating authority in the sphere of medical devices, has …

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 …

Custom-made medical devices in Great Britain - GOV.UK

https://www.gov.uk/government/publications/custom-made-medical-devices

Medical devices regulation and safety Guidance Custom-made medical devices in Great Britain How to comply with the regulatory requirements for …

MHRA guidance on registration and deadlines for medical …

https://www.emergobyul.com/news/uk-mhra-issues-post-brexit-medical-device-ivd-registration-requirements

On or before their applicable registration deadlines, device manufacturers must submit company, device and UK Responsible Person (UKRP) information to MHRA …

Login - Device Registration - MHRA

https://aic.mhra.gov.uk/era/drsystem.nsf/login

Welcome to MHRA’s On-line Registration System This system has been especially designed by the MHRA to provide device manufacturers, assemblers and their authorised …

UK MHRA Medical Device Regulations: and IVD Products | NAMSA

https://namsa.com/uk-mhra-medical-device-regulations-impact-to-ivd-manufacturers/

The MHRA proposals for grace periods for existing UKCA, IVDR and IVDD certificates and declarations will certainly be welcome by IVD manufacturers, and provide …