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Description

In this episode of the Global Medical Device Podcast, host Etienne Nichols delves into the intricate world of in vitro diagnostics (IVDs) with Christie Hughes, a principal consultant and IVD expert at Qserve Group. With over 25 years of experience, Christie shares her extensive knowledge, discussing the nuances of IVDs, regulatory landscapes, and practical insights for professionals transitioning into or within the IVD sector.

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Key Takeaways:

  1. Trends in MedTech: The regulatory environment for IVDs is rapidly evolving, with increased scrutiny and changes in compliance requirements globally.
  2. Practical Tips: For those entering the IVD field, familiarize yourself with FDA decision summaries and EUA documentation to understand current regulatory expectations.
  3. Future Predictions: Expect continued integration of IVDs with digital health technologies, raising both opportunities and regulatory complexities.

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MedTech 101:

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This episode is brought to you by Greenlight Guru, a quality management system and electronic data capture software designed...