Clinical Login Support
Products

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

Learn More

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.

View Product Tour

Data collection and management designed for MedTech clinical trials.

Learn More

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

Get a personalized demo of Greenlight Guru Clinical today.

Request a Demo
Solutions
Why Us
Customers
Partners
Company
Resources
BestQMS-book-mockup-01

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.

View Now
Pricing
Contact Sales Get a Demo
Contact Sales
Get a Demo

FREE ON-DEMAND WEBINAR
October 10, 2023 at 3:00 PM CEST / 9:00 AM EDT

Data Management and Monitoring in MedTech Clinical Studies

Join us for a compelling discussion on the pivotal roles of data management and monitoring within MedTech clinical studies. This panel session offers a unique opportunity to delve into the nuances of monitoring and data management to learn how to navigate the challenges these crucial areas present.

Hear from experts at Avania and Boston Medtech Advisors as they share best practices, highlight common pitfalls, and discuss the evolving landscape of remote versus on-site monitoring.

Near the end of the panel, our product expert will provide insights on how the new Greenlight Guru Clinical Reporting module can improve data management and monitoring workflows by bringing all critical data into one convenient view. This new module streamlines clinical data management processes, allows teams to make informed decisions faster, and saves countless hours of work.

Watch for free
GG Avania & BMTA Reporting webinar 2023 thumbnail
Key takeaways:
  • Best practices for data management in MedTech clinical studies
  • How to overcome the most resource-intensive obstacles in monitoring
  • Remote monitoring vs. on-site
  • Data management pitfalls and timesavers
  • How Greenlight Guru Clinical’s new Reporting module streamlines data management & monitoring processes
Who should attend?
  • Clinical Affairs Professionals and Management
  • Clinical Operations Professionals and Management
  • Medical Device Executives
Register Now  

Hosted by

Chris Rush headshot1
Moderator:
CHRIS RUSH

Solutions Engineer,
Greenlight Guru Clinical
sara little - bmt
Speaker:
SARA LITTLE

Senior Consultant,
Boston MedTech Advisors
Saskia Yperlaan
Speaker:
SASKIA YPERLAAN

Clinical Research Associate,
Avania
Matthijs Hermse - Avania
Speaker:
MATTHIJS HERMSE

Senior Data Analyst,
Avania

Greenlight Guru logo

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.

About Boston Medtech Advisors

Founded in 2004, Boston MedTech Advisors has worked with more than 350 medical technologies and life sciences companies. BMTA supports clients to commercialize new products and services and increase their market adoption by addressing their unique and inter-dependent regulatory, clinical, reimbursement, marketing and business development requirements.

The company's wide range of experience across these areas provides clients with comprehensive strategies that take both regulatory and market factors into consideration. 

Visit their website to learn more.

avania-logo

About Avania

Avania is the team that has the regional experience and global expertise to take your product from feasibility all the way through post-approval. Avania is dedicated to driving your product forward. When you partner with Avania, you become part of a company legacy built on more than 30 years of experience.

Avania brings knowledgeable experts together to form a unique CRO that can advance the research of medical devices, novel technology, and combination products. All of this is available across a wide range of therapeutic specialties. This ensures you receive the kind of customized, scalable solutions that will optimize efficiencies and streamline the advancement of your medical technology. And since Avania’s experts are known for providing transparent, open communication, you’ll always have complete project visibility whenever you need it. 

Visit their website to learn more.

Featured In