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Webinar: How you need to modernize your medical device records

November 20, 2019 By Kim Dorsey

This webinar was presented live on Wednesday, December 11, 2019. Click below to watch it on demand.

 

 

When manufacturers employ manual, paper-based systems to manage their production records, human errors and poor data integrity have a cascading effect as the data advances through the production process, slowing everything down. To compete in a modern market, manufacturers can no longer rely on manual, paper-based systems to manage quality and production, largely due to this ripple effect.

Managing paper in a digital world means bad data, not big data, on the shop floor. In this session, attendees will discover how and why digital device history records (DHRs) enable medtech manufacturers to intelligently identify, surface, filter and act on data from throughout production.

Attendees of this webinar will learn:

  • How Industry 4.0 will affect device history records (DHRs).
  • Hidden costs of paper-based or partially electronic DHRs.
  • What a truly paperless DHR environment looks like.
  • Real-world benefits of digitizing the DHR process.

Featured Speakers:

Dave Edwards
Executive Vice President
MasterControl

 

 

Danielle Kirsh
Senior Editor
Medical Design and Outsourcing

 

 

 

Sponsored by:

 

 

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  • Home
  • Medical Device Business
    • Mergers & Acquisitions
    • Financial
    • Regulatory
  • Applications
    • Cardiovascular
    • Devices
    • Imaging
    • Implantables
    • Medical Equipment
    • Orthopedic
    • Surgical
  • Technologies
    • Contract Manufacturing
    • Components
    • Electronics
    • Extrusions
    • Materials
    • Motion Control
    • Prototyping
    • Pumps
    • Tubing
  • Med Tech Resources
    • DeviceTalks Tuesdays
    • Digital Editions
    • eBooks
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    • MedTech 100 Index
    • Podcasts
    • Print Subscription
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    • Video
  • 2022 Leadership in MedTech
    • 2022 Leadership Voting!
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