398 Folgen

  1. Explaining the Role of Importer under EU MDR

    Vom: 1.7.2021
  2. Preparing Your Pre-Submission with the Content FDA Wants to See

    Vom: 23.6.2021
  3. How RADx Tech II Program is Fast-Tracking COVID-19 Technologies to Market in 2021

    Vom: 21.6.2021
  4. How New Training Partnership is Advancing Medical Device Knowledge & Professional Development

    Vom: 16.6.2021
  5. Top 3 Most Cited Issues in Medical Device Inspections from FDA FY2020

    Vom: 14.6.2021
  6. How Mindset Training Can Help Your Team Operate at Peak Performance

    Vom: 10.6.2021
  7. Examining the HHS Proposal for Premarket Notification Exemptions

    Vom: 7.6.2021
  8. Crash Course on Greenlight Guru Academy: How Medical Device Professionals Stay Ahead

    Vom: 2.6.2021
  9. Building your Brand as a Medical Device Professional

    Vom: 31.5.2021
  10. Understanding the Value of a Medical Device Guru

    Vom: 26.5.2021
  11. Meet a Guru: Etienne Nichols

    Vom: 24.5.2021
  12. Meet a Guru: Laura Court

    Vom: 19.5.2021
  13. Regulatory Tips & Pointers from a Former FDA Reviewer

    Vom: 17.5.2021
  14. Why Demand is so High for Regulatory & Quality Jobs (and should you take advantage?)

    Vom: 12.5.2021
  15. Comparing FDA’s Breakthrough Devices Program & Safer Technologies Program

    Vom: 11.5.2021
  16. Why is IVDR Causing Widespread Panic throughout the Medical Device Industry?

    Vom: 7.5.2021
  17. Managing Business Risk as a Medical Device Company

    Vom: 3.5.2021
  18. Waterfall vs. Agile: Battle of the Product Development Methodologies

    Vom: 28.4.2021
  19. For the Love of Internal Auditing

    Vom: 27.4.2021
  20. Similarities & Differences between In Vitro Diagnostic (IVD) Devices & Medical Devices

    Vom: 21.4.2021

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