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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 20, 2024

Integrating Clinical Strategy and Project Management for Cost-Effective Clinical Investigations

The focus of this webinar is to help medical device professionals run cost-effective and successful clinical investigations.

Although cost-effective and successful may not always be compatible, focusing on important aspects early in the preparation phase of a clinical investigation is crucial.

These aspects include: clinical strategy, clinical study design, clinical project management, and data management. Prioritizing and getting these right early on, can reduce the likelihood of issues occurring during a clinical study.

Using a case study approach, Bianca Lutters, Head of Clinical Operations, and Caesar Roseboom, Clinical Project Manager at Qserve, will join forces with Chris Rush, Solutions Engineer at Greenlight Guru.

Together, they will discuss how those aspects can help medical device companies run a compliant clinical investigation that results in high-quality data and fewer delays.

Watch for free
Specifically, this webinar will cover:
  • Why starting early with the clinical strategy and clinical investigation design is beneficial
  • The importance of site and country selection for both timelines and data quality in your study
  • How a proper set-up of your database and data management are key for the collection of high-quality data
Who should attend?
  • Clinical Affairs Professionals and Management
  • Clinical Operations Professionals and Management
  • Clinical Researchers and Project Managers
  • Regulatory Professionals and Management
  • Medical Device Executives
Register Now  

Hosted by

Etienne-Nichols-round
Moderator:
ETIENNE NICHOLS

Medical Device Guru,
Greenlight Guru
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Speaker:
BIANCA LUTTERS

Head of Clinical Operations,
Qserve
Chris Rush headshot1
Speaker:
CHRIS RUSH

Solutions Engineer,
Greenlight Guru
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Speaker:
CAESAR ROSEBOOM

Clinical Project Manager,
Qserve

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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 Qserve

Our mission is to help improve patient safety and health by supporting the advancement of biomedical technology. We assist medical device and in-vitro diagnostics manufacturers worldwide with market access, medical device approvals, clinical trials and achieving and maintaining regulatory compliance. 

We are passionately working for our customers on regulatory, quality and clinical challenges and see it as our responsibility to create a diverse global team of professionals who share the same passion for medical device technology, a high standard of quality, competence and customer service, and enjoy the fun of working on this together every day.

Visit their website to learn more.

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