#In Vitro Diagnostic Medical Devices (IVDMD)

ResultsFound 9 items

Guide

November 27, 2019

Notified Bodies: Certifying Your Products Under the EU Medical Device Regulation

This guide explores the role of notified bodies, the process toward certifying products under the ne...Continue Reading

Guide

November 12, 2019

Managing Requirements Under Section 10.4 of the EU Medical Device Regulation

Section 10.4 of the EU MDR expands on the past definition of medical devices, bringing more products...Continue Reading

Webinar

December 5, 2018

Preparing for the New EU Medical Device Regulation

The upcoming European Union (EU) Medical Device Regulation (MDR) will replace the Medical Devices Di...Continue Reading

Webinar

May 14, 2019

Ask the Experts: Preparing for the European Union Medical Device Regulation

The European Union (EU) Medical Device Regulation (MDR) is set to come into effect on May 26, 2020, ...Continue Reading

Guide

June 12, 2019

The Assent Solution for Medical Device Companies

This guide outlines Assent's solution for medical device companies as they manage unique requirement...Continue Reading

eBook

June 12, 2019

Understanding the European Union Medical Device Regulation

This eBook provides information on implementing the new EU MDR to maintain market access, and certif...Continue Reading

eBook

June 12, 2019

Navigating the Compliance Landscape: Medical Devices

This eBook offers valuable information on the product compliance, corporate social responsibility an...Continue Reading

Article

May 17, 2017

EU Medical Device Regulation

The Medical Device Regulation (EU) 2017/745 establishes a regulatory framework for medical devices t...Continue Reading

© 2020 Assent Compliance Inc.