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Clinlogix to share details on recording serious adverse events in device testing

November 16, 2020 By Tom Salemi

Safety is always a paramount concern, especially as medical devices, combination products, and in-vitro diagnostics (IVD) become increasingly important in the management and delivery of patient care

Now more than ever, having the proper framework for the collection and reporting of safety data to ensure both patient safety and efficacy during a clinical trial is essential.

On Tuesday, Nov. 17 at 4 pm ET, Clinlogix’ Jen Kratz, director of safety services, and Solange Bishop, clinical data manager, will present the more pressing challenges of recording adverse events.

During this presentation attendees will learn about the challenges and best practices for medical device clinical trial Safety Management, including Severe Adverse Event (SAE) data capture and cleaning to ensure uniform data for regulatory submissions and clinical data analysis.

Go here to register for this DeviceTalks Tuesdays event.

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Search Medical Design & Outsourcing

  • 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
    • Manufacturer Search
    • Medical Device Handbook
    • MedTech 100 Index
    • Podcasts
    • Print Subscription
    • The Big 100
    • Webinars / Digital Events
    • Whitepapers
    • Video
  • 2022 Leadership in MedTech
    • 2022 Leadership Voting!
    • 2021 Winners
    • 2020 Winners
  • Women in Medtech