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More than a Quality Management System: Tools for the entire MedTech Lifecycle.

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Featured Capabilities:

Document Management Training Management Product Development Design Control Risk Management CAPA Management Audit Management

Experience the #1 QMS software for medical device companies first-hand. Click through an interactive demo.

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Data collection and management designed for MedTech clinical trials.

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Featured Capabilities:

Electronic Data Capture (EDC) Electronic Case Report Forms (eCRF) Electronic Patient Reported Outcomes (ePRO) Ad-Hoc Data Collection (Cases) Post-Market Surveys Product Add-Ons

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Ultimate Guide to Comparing Quality Management System Solutions

This eBook compares the best QMS software solutions to help medical device companies make an informed decision when investing in a quality management system.

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FREE ON-DEMAND WEBINAR
March 19, 2024

Insights from TÜV SÜD and Greenlight Guru on the Requirements of PMCF under the MDR 2017/745

PMCF requirements have been part of the directives, but became more detailed under the EU MDR.

The MedTech industry has been looking for inspiration for how to comply with the MDR regarding post-market clinical follow up data.

PMCF clinical investigation is one method explained in the MDR, but medical device manufacturers should determine which method is suitable for their device.

In this webinar, experts from TÜV SÜD and Greenlight Guru will explore examples of PMCF methods. Sign up to get a better understanding of PMCF.

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Insights from TÜV SÜD and Greenlight Guru on the Requirements of PMCF under the MDR 2017745
This webinar will cover:
  • Insights and key considerations from TÜV SÜD and Greenlight Guru, on PMCF requirements
  • Alternative PMCF methods and when to use them
  • Live Q&A
Who should attend?
  • Clinical Affairs Professionals and Management
  • Clinical Operations Professionals and Management
  • Clinical Research Professionals and Management
  • Medical Device Executives
Register Now  

Hosted by

Laura Court
MODERATOR:
LAURA COURT

Solutions Engineer,
Greenlight Guru
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PRESENTER:
RENE BOMBIEN

Chief Medical Officer
TÜV SÜD Denmark MHS
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PRESENTER:
CHRIS RUSH

Solutions Engineer,
Greenlight Guru

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About Greenlight Guru

Greenlight Guru is the leading connected, cloud-based platform purpose-built for MedTech companies. The end-to-end solution streamlines product development, quality management, and clinical data management by integrating cross-functional teams, processes, and data throughout the entire product lifecycle.

Greenlight Guru’s platform is used by organizations across the globe that are replacing their disjointed, legacy tools and solutions to bring life-changing products to people faster and with less risk.

Visit our homepage to learn more.

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About TÜV SÜD

TÜV SÜD is a trusted partner of choice for safety, security and sustainability solutions. It specialises in testing, certification, and auditing services.

Through more than 26,000 employees across over 1,000 locations, it adds value to its customers, inspiring trust in a physical and digital world.

Visit their homepage to learn more.

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