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Resource Library for Medical Device Professionals

11 total results. Show all resources.
Register for our free webinar on choosing or changing your EU Notified Body
Europe

WATCH NOW: How to Select or Change Your EU Notified Body

In this recorded webinar we will tell you how to deal with the issue of transitioning to another Notified Body and/or how to evaluate your options in establishing a new relationship.

1 hour
Jan 4, 2017
Emergo MDR webinar October 2017
Europe

WATCH NOW: The new European Medical Devices Regulation (MDR 2017/745)

In this webinar, we outline the most important MDR changes you need to know.

1 hour
Sep 15, 2017
Register: Eudamed Webinar July 2018
Europe | In-Vitro Diagnostic Devices, | Medical Devices

WATCH NOW: Eudamed Requirements under the EU MDR and IVDR

In this one-hour webinar, Ronald Boumans discusses the role of Eudamed in MDR/IVDR compliance.

1 hour
Jun 12, 2018
How device companies can prepare for a no-deal Brexit
Europe

WATCH: Impact of a No-Deal Brexit

1 hour
Jan 31, 2019
Register for our free webinar on Transitioning to ISO 13485:2016
Europe

WATCH NOW - What You Need To Know about ISO 13485:2016

In this recorded webinar we cover the major changes that have been made and tell you what needs to be done before you seek recertification by your Notified Body.

1 hour
Dec 15, 2016
Register for our webinar: Post Market Surveillance & PMCF under the European MDR
Europe

WATCH NOW: PMS & PMCF under the European MDR

Europe's new Medical Devices Regulation (MDR) adds to the complexity of complying with specific PMS and post-market clinical follow-up (PMCF) requirements. In this free webinar, we discuss new European PMS and PMCF requirements.

1 hour live webinar
Apr 10, 2017
Conducting a medical device PMCF webinar
Europe | Medical Devices

WATCH NOW: Conducting a Medical Device PMCF Study

In this webinar, you'll learn what it takes to conduct a compliant Post-Market Clinical Follow-up study for your medical device.

1 hour
Oct 4, 2018
Webinar - GDPR and its impact on human factors studies
Europe | Medical Devices

REGISTER NOW: GDPR and its impact on Human Factors studies

In this webinar, we discuss GDPR compliance considerations for human factors professionals.

1.5 hours
Feb 19, 2019
14971 risk management webinar
Europe | Medical Devices

WATCH NOW: Risk Management according to EN ISO 14971:2012

This free recorded webinar is about risk management for medical device companies according to EN ISO 14971:2012.

One hour
Aug 10, 2017
Watch our recent webinar on the European In Vitro Diagnostic Devices Regulation
Europe

WATCH NOW: Europe's New IVDR 2017/746

Within the next few years, the regulatory landscape will change dramatically for IVD companies selling in Europe. IVDR 2017/745 will be an entirely new classification scheme for IVDS, and places far more emphasis on clinical data and risk management

1 hour
Nov 18, 2016
CER Complience webinar EMERGO 2018
Europe

WATCH NOW: Ensure Your CER Complies with MEDDEV 2.7/1 v4

In this webinar, we outline what you need to know about writing a compliant EU Clinical Evaluation Report.

1 hour
Jan 29, 2018