EU Notified Bodies designated under the EU MDR (2017/745)

In this blog, we have listed the EU MDR notified bodies designated under the EU Medical Devices Regulation (MDR). We will keep this list updated as and when a new Notified Body is added.

Previous
Next

Comments

Leave a Comment

Latest Blog

HUMAN ERROR

Role of Human Errors in CAPAs

FDA Guidance on SaMD

FDA Guidance on SaMD

Challenges in writing Clinical Evaluation Reports

Challenges in writing Clinical Evaluation Reports

Investigation and Root cause analysis

Investigation and Root cause analysis

NCs in medical device industry

NCs in medical device industry

Pharma industry and NCs

Pharma industry and NCs

Broad Spectrum for Non conformance

Broad Spectrum for Non conformance

EU Notified Bodies Designated Under the EU MDR.

SARACA's success in the Aerospace and Defense (A&D) Industry.

Key highlights of the revised Swiss Medical Device Ordinance

The Helsinki procedure for borderline and combination medical devices

Unique ID for Clinical Investigations under MDR

Guidance on the key changes of classification rules under the European Medical Devices Regulation

Can you continue your legacy medical device in EU MDR without adequate clinical data?

The creation of a Design History File (DHF) Per 21 CFR 820.30

The Performance Evaluation Report (PER) Per (EU) 2017/746

Major ISO 14971:2019 Changes That All Users and Manufacturers Should Know.

A Strategy for Responding Appropriately to FDA.

Best Practices for Storing Data Intelligently for Faster CER Updates

Are You Paying Exorbitantly for Your Quality and Regulatory Consultants.

We use cookies to ensure you get the best experience on our website. By clicking “Accept Cookies” you agree to our use of cookies. Learn More
Reject Accept