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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
August 13, 2024

EU MDR Hot Takes: Evolution or Overreach?

Join us for a lively and informal conversation featuring industry experts Karandeep Singh Badwal and Michelle Lott, with Etienne Nichols moderating.

In this engaging session, we'll delve into the differing views on the EU MDR regulations. One side argues that these rules have always been implied, essential for ensuring patient safety and product effectiveness. The other side believes that EU MDR has gone too far, placing undue burdens on medical device companies, stifling innovation, and inflating costs.

Don't miss this opportunity to hear diverse perspectives and engage in a thought-provoking discussion, ask questions, and gain valuable insights on navigating these regulatory changes effectively.

Specifically, This webinar will:
  • Understanding the EU MDR Framework: Gain a clear understanding of the key components and intentions behind the EU MDR regulations, and how they compare to previous standards.
  • Impact on Medical Device Companies: Explore the practical implications of EU MDR on medical device companies, including compliance challenges, cost implications, and effects on innovation.
  • Strategies for Effective Navigation: Discover actionable strategies and best practices for navigating the EU MDR landscape, ensuring compliance while maintaining agility and innovation in product development.

Watch the webinar
EU MDR Hot Takes_Evolution or Overreach
Who should attend?
  • Product Development Professionals and Management
  • Quality Professionals and Management
  • Regulatory Professionals and Management
  • Medical Device Executives
Register Now  

Hosted by

Etienne-Nichols-round
Moderator:
Etienne Nichols

Head of Industry Education & Insights,
Greenlight Guru
Michelle Lott - white background
Presenter:
Michelle Lott

Principal and Founder,
leanRAQA
Karandeep Badwal
Presenter:
Karandeep Badwal

Founder, QARA Consultant,
QRA Medical

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About Greenlight Guru

Greenlight Guru is the leading cloud-based platform purpose-built for MedTech companies. The end-to-end solution goes beyond traditional QMS needs by integrating cross-functional teams, processes, and data throughout the entire product lifecycle so device makers can proactively overcome execution gaps, streamline compliance, and accelerate market success.

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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