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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
April 16, 2024

Revolutionizing Medical Device Trials with Risk-Based Monitoring

Join this webinar where Helene Quie and Chris Rush will unveil the power of Risk-Based Monitoring (RBM) in revolutionizing medical device clinical studies. RBM shifts the paradigm from traditional monitoring to a proactive strategy focused on early risk identification and mitigation.

Learn how this approach not only meets the unique challenges of medical device trials but also enhances patient safety, data integrity, and accelerates study timelines and market access for groundbreaking innovations.

Helene, CEO at Qmed Consulting, will offer invaluable insights from real-world case studies showcasing RBM's success. She will also discuss how to navigate the complexities of its adoption, share best practices, and peek into the future with emerging trends and technologies shaping RBM.

Complementing Helene's strategic overview, Chris Rush, Solutions Engineer at Greenlight Guru will focus on the technical aspects of RBM. He will discuss ways to reduce risks related to clinical activities and how to leverage software-based solutions for more efficient and effective risk management.

 

Register for free
Revolutionizing Medical Device Trials with Risk-Based Monitoring
Key takeaways:
  • Challenges and best practices in adopting RBM for medical devices
  • Future directions and emerging trends in RBM for medical device clinical studies
  • Greenlight Guru's insights on reducing risk related to clinical activities
  • Software based approaches to risk based monitoring
Who should attend?
  • Clinical Affairs Professionals and Management
  • Clinical Operations Professionals and Management
  • Regulatory & Quality Professionals and Management
  • Medical Device Executives
Register Now  

Hosted by

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Moderator:
ETIENNE NICHOLS

Medical Device Guru,
Greenlight Guru
Helene Quie round
Speaker:
HELENE QUIE

CEO,
Qmed Consulting
Chris Rush headshot1
Speaker:
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 Qmed Consulting

Founded in 2006 by Helene Quie, Qmed Consulting is a full-service Contract Research Organization (CRO) based near Copenhagen, Denmark. We provide strategic consulting services in connection with device approval in Scandinavia and internationally through our global alliance.

The driving force behind Qmed Consulting is our commitment to clearing the path for new medical devices and new ideas based on project management, best-in-class expertise in clinical trials, clinical development, regulatory affairs, quality management and commercial healthcare.

When you partner with Qmed Consulting, you acquire direct access to our team of highly skilled professionals. Our team has more than 100 years of experience working in the field of medical device and IVD approval.

Visit their website to learn more.

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