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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

How and When to Start Documenting Your Design Controls with DHF Ready Ideation

Design history file (DHF) Ready Ideation is a toolset that encourages creative, evolutionary, and holistic design while at the same time building the foundation for formal design controls. 

DHF Ready Ideation reduces the cost of retrospectively assembling a design history, makes the process of designing a medical device enjoyable, and reveals relationships across multiple business and technical perspectives that are typically difficult to realize.

During this free 60 minute webinar presented by Andrew DiMeo, Sr., Ph.D., Innovation & Design Coach at Trig, you will learn how to determine the best time to start documenting your design controls to improve product development through an innovative and proven approach known as DHF Ready Ideation.

Watch the webinar
Webinar Trig - DHF Ready Ideation
Specifically, this webinar will cover:
  • How early is too early to start design controls?  When is late, too late?
  • Reducing the pain of turning on design controls
  • The medical device diligence dashboard
  • The waterfall process reimagined as iterative
  • Prototyping and human factors engineering
  • A visual approach to risk management
  • Q&A Session
Who Should Attend?
  • Medical Device Executives
  • Regulatory Affairs Professionals and Management
  • Quality Professionals and Management
  • Clinical Affairs Professionals and Management
  • R&D Engineers and Management
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Hosted by

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Presenter: Andrew DiMeo

Innovation & Design Coach, Trig
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Moderator: Jon Speer

Founder & VP QA/RA, Greenlight Guru

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About Trig
Trig is a full service industrial design firm serving the consumer, healthcare, and durable goods markets. Their comprehensive innovation process includes insights and ideation, product design, and brand asset management agency for start-ups, mid-sized, and Fortune 500 companies across the United States.  Based in Chapel Hill, the Trig® product design consulting team can be found in Charlotte, Raleigh, and Richmond, Virginia. Visit their website to learn more.

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About Greenlight Guru

Greenlight Guru is the only Medical Device Success Platform (MDSP) for companies to bring new products to market faster while simplifying regulatory compliance and reducing risk. Being the only industry specific, cloud-based software, Greenlight Guru is easier to implement, easier to use and designed to fit all medical device needs to enable innovative, safe and effective, True Quality medical devices. Visit our homepage to learn more.

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