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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
January 31, 2024

Key Elements to Outsourcing Clinical Activities in 2024

Join us for this enlightening webinar where we will delve into critical insights and strategies essential for MedTech professionals involved in outsourcing or insourcing clinical studies.

Whether you're contemplating outsourcing for the first time or looking to refine your existing strategies, this webinar will offer fresh perspectives and actionable advice.

During the webinar, our speakers will discuss what aspects of your clinical studies can be effectively outsourced and what should be kept in-house. This is crucial for making informed decisions that align with your organization's goals and regulatory standards.

Aditionally, Greenlight Guru's Natalie Logeman (Senior Manager, Partnerships) will share valuable advice for working seamlessly with Contract Research Organizations (CROs), and offer a blueprint to help you establish productive partnerships and ensure the success of your clinical projects.

Watch for free
Key Elements to Outsourcing Clinical Activities in 2024
This webinar will cover:
  • Key results from Greenlight Guru's comprehensive industry survey
  • What you need to know about outsourcing/insourcing your clinical studies
  • What can be outsourced and what can't
  • Cheat Sheet for working with CRO partners
Who should attend?
  • Clinical Affairs Professionals and Management
  • Clinical Operations Professionals and Management
  • Medical Device Executives
  • Clinical Research Professionals and Management
Register Now  

Hosted by

Etienne-Nichols-round
MODERATOR:
ETIENNE NICHOLS

Medical Device Guru,
Greenlight Guru
Natalie Boone
PRESENTER:
NATALIE LOGEMAN

Senior Manager, Partnerships
Greenlight Guru
Chris Rush headshot1
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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