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Torstaisin

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393 Jaksot

  1. Understanding the Investigational Device Exemption (IDE) Process

    Julkaistiin: 31.3.2021
  2. Evaluating, Monitoring & Selecting Suppliers in the Medical Device Industry

    Julkaistiin: 30.3.2021
  3. Why the PMA Process is so Dreaded by Manufacturers in the US Market

    Julkaistiin: 25.3.2021
  4. Learning about the Real-world Impact of Design, Manufacturing, Quality & Culture on Patients

    Julkaistiin: 24.3.2021
  5. What is the Safer Technologies Program (STeP) and Can Your Device Use It?

    Julkaistiin: 21.3.2021
  6. Meet a Guru: Sara Adams

    Julkaistiin: 17.3.2021
  7. Building a Startup in the MedTech Industry

    Julkaistiin: 10.3.2021
  8. Meet a Guru: Karen Schuyler

    Julkaistiin: 8.3.2021
  9. Visualizing a Medical Device through Illustrations, Animations, and other Artwork

    Julkaistiin: 4.3.2021
  10. Everything you Need to Know about SaMD from an FDA Perspective

    Julkaistiin: 1.3.2021
  11. Preparing for Remote and On-Site Inspections and Audits

    Julkaistiin: 24.2.2021
  12. How does EU MDR impact your Quality Management System?

    Julkaistiin: 22.2.2021
  13. Virtual Auditing in a Post-COVID World of Digital Compliance

    Julkaistiin: 18.2.2021
  14. Inside Look into ISO 14971:2019 & ISO TR 24971:2020 from the Author's Point of View

    Julkaistiin: 10.2.2021
  15. Prioritizing Medical Device Reimbursement During Product Development

    Julkaistiin: 4.2.2021
  16. 5 Actionable Lessons Learned from the RADx Initiative by NIH

    Julkaistiin: 27.1.2021
  17. What are the Strategic Priorities for CDRH in 2021?

    Julkaistiin: 20.1.2021
  18. Understanding and Handling Different Types of Feedback

    Julkaistiin: 14.1.2021
  19. Measuring the Impact of AI/ML Technologies on the Current Medical Device Landscape

    Julkaistiin: 7.1.2021
  20. Post-Pandemic Readiness: Preparing for the Aftermath of COVID-19 on the Medical Device Industry

    Julkaistiin: 23.12.2020

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