Gefragt von: Daniel Alexiuc
Fragesteller Allgemeines

Mhra Portal Medical Device

Der Link der Mhra Portal Medical Device-Seite ist unten angegeben. Seiten, die sich auf Mhra Portal Medical Device beziehen, werden ebenfalls aufgelistet.

Zuletzt aktualisiert: 2022-02-04

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

31.12.2020 · The following devices in Great Britain (England, Wales and Scotland) need to be registered with the MHRA under existing arrangements: Class I medical devices IVDs (including all IVDs undergoing...
Url: https://www.gov.uk/guidance/register-medical-devices-to-place-on-the-market
Register medical devices to place on the market - GOV.UK

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Public Access Database for Medical Device Registration

201 Zeilen · Registration does not represent any form of accreditation, certification or approval …
Url: https://aic.mhra.gov.uk/era/pdr.nsf/name?openpage&start=1&count=200
Public Access Database for Medical Device Registration

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Notify the MHRA about a clinical investigation for a ...

18.12.2014 · How to notify the MHRA of your clinical investigation. A notification to the MHRA will not be required for medical devices that are UKCA / CE / …
Url: https://www.gov.uk/guidance/notify-mhra-about-a-clinical-investigation-for-a-medical-device
Notify the MHRA about a clinical investigation for a ...

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Regulating medical devices in the UK - GOV.UK

Url: https://www.gov.uk/guidance/regulating-medical-devices-in-the-uk
Regulating medical devices in the UK - GOV.UK

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Login - Device Registration - MHRA

You must re-register all your medical devices on the new MHRA Online Registration System. For more details, please see our published registration guidance. This system has been especially designed by the MHRA to provide device manufacturers, assemblers and their authorised representatives, a simple electronic means of registering with the Agency.
Url: https://aic.mhra.gov.uk/era/drsystem.nsf/login
Login - Device Registration - MHRA

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Medical devices: guidance for manufacturers on vigilance ...

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

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MHRA New Medical Device Regulations | RegDesk

03.09.2020 · The MHRA guidance also provides details regarding the applicable legislative acts establishing the rules and requirements in the sphere of medical devices. Nowadays, the legal framework includes: The Directive 90/385/EEC on active implantable medical devices (AIMDD), The Directive 93/42/EEC on medical devices (MDD), and
Url: https://www.regdesk.co/mhra-new-mdr/
MHRA New Medical Device Regulations | RegDesk

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MHRA - MHRA Portal

View the Terms & Conditions of use for the MHRA Portal ...
Url: https://info.mhra.gov.uk/mhra_portal.aspx
MHRA - MHRA Portal

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Register to make submissions to the MHRA - GOV.UK

31.12.2020 · For further information, please email our Customer Services Centre at [email protected] or call 020 3080 6000. You can also email [email protected] with urgent questions. Alternatively ...
Url: https://www.gov.uk/guidance/register-to-make-submissions-to-the-mhra
Register to make submissions to the MHRA - GOV.UK

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Medical device regulation and the MHRA devices registration system

Medical device regulation and the MHRA devices registration system

Added by: MHRAgovuk

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EU Exit and post-transition guidance, Regulation of Medical Devices Webinar - October 2020

EU Exit and post-transition guidance, Regulation of Medical Devices Webinar - October 2020

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MHRA Innovation Office

MHRA Innovation Office

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European Medical Device Registration Chapter 1 - Overview

European Medical Device Registration Chapter 1 - Overview

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The role of the Medicines and Healthcare Products Regulatory Agency

The role of the Medicines and Healthcare Products Regulatory Agency

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Recording of the medical devices consultation webinar – Industry 5 October 2021

Recording of the medical devices consultation webinar – Industry 5 October 2021

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MHRA continues to issue new guidance for medical devices

MHRA continues to issue new guidance for medical devices

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Webinar // UKCA Requirements for Medical Device Manufacturers

Webinar // UKCA Requirements for Medical Device Manufacturers

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European Medical Device Registration Chapter 2 - Classification

European Medical Device Registration Chapter 2 - Classification

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How to register Covid19 Medical Supplies? [Case Study UK MHRA]

How to register Covid19 Medical Supplies? [Case Study UK MHRA]
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