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

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Featured Capabilities:

Document Management Product Development Design Control Risk Solutions Training Management CAPA 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

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Learn valuable, career-boosting skills for the Medical Device industry. Get access to hundreds of free resources as well as subscription-based courses and certifications.

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FREE ON-DEMAND WEBINAR

5 Predictions for the Medical Device Industry in 2018 (And How You Can Prepare)

What should the medical device industry expect in 2018?

Great question.

From ISO 13485 being revised in 2016, the EU MDR / IVDR being revised in 2017, and the MDSAP program going live in 2017, regulatory changes have been rampant and significant for medical device professionals.

In this free 60 minute webinar, Jon Speer, a 20+ year medical device industry veteran and founder & VP QA/RA at Greenlight Guru will be sharing some of his insights and observations for the upcoming year based on data and trends.

Join this webinar to stay one step ahead of the competition and learn how you can begin preparing for all the changes in store for 2018.

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Specifically, you will learn:
      • Why you should expect it to be harder for devices to get to market and stay there in the EU
      • How to avoid the mad dash to update ISO 13485 certification before the deadline
      • Where the latest revision of ISO 14971 is and when to expect the next update
      • About Health Canada and their MDSAP deadline
      • Why companies are shifting from being compliance-focused to quality-focused 
Who Should Attend?
      • Medical Device Executives
      • Quality Assurance and Quality Control
      • Regulatory Affairs and Compliance
      • Manufacturing
      • Supplier Management
      • Internal, External and Quality Auditors
      • Document Control
      • Production
      • Operations
      • Suppliers to the Medical Device Industry
      • R&D / Product Development

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Moderator/Presenter: Jon Speer

Founder, Greenlight Guru
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About Greenlight Guru

Greenlight Guru is the only quality management software platform designed specifically for medical device companies. The platform helps companies bring safer products to market faster, simplifies FDA and ISO regulatory compliance and provides a single source of truth by connecting the management of all quality processes like CAPAs, risk, audits and more. Greenlight Guru’s platform is used by thousands of users across the globe to push beyond baseline compliance and achieve True Quality for their medical devices.

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