416 Odcinki

  1. Integrating Business Elements into Your Product Development Process with Therese Graff

    Opublikowany: 7.11.2019

  2. Tips to Help You Prepare for an FDA Inspection

    Opublikowany: 7.11.2019

  3. What Device Makers Need to Know About Design Verification and Validation with Mike Drues

    Opublikowany: 7.11.2019

  4. Preparing Your Class II Device for the UDI Compliance Deadline with Gary Saner

    Opublikowany: 7.11.2019

  5. Dirty Devices and Reprocessing: Are New Design Change Rules On the Horizon?

    Opublikowany: 7.11.2019

  6. Insider Tips and Best Practices Regarding the 510(k) Submission Process from a Former FDA Reviewer

    Opublikowany: 7.11.2019

  7. Insights Into the New FDA 3D Printing Guidance & How It Impacts Med Device New Product Development

    Opublikowany: 7.11.2019

  8. How to Properly Use the FDA Pre-Submission Process and Why It's So Important with Mike Drues

    Opublikowany: 7.11.2019

  9. Tips & Pointers for Effective Internal Quality Audits with Kyle Rose

    Opublikowany: 7.11.2019

  10. Preparing for the Changes to the EU Medical Device and In-Virto Diagnostics Regulations

    Opublikowany: 7.11.2019

  11. Tips for Avoiding Problems with the First-In-Human Study Process with Mike Drues

    Opublikowany: 7.11.2019

  12. Understanding the New FDA Guidance on Changes to 510(k)

    Opublikowany: 7.11.2019

  13. What Devicemakers Need to Know about the FDA Pre-submission Process (Part Two)

    Opublikowany: 7.11.2019

  14. Zebra Medical Technologies: How a New Breed of Medical Device Companies Is Leveraging Technology

    Opublikowany: 7.11.2019

  15. Tips for Success When It Comes to IEC 60601 with Leo Eisner

    Opublikowany: 7.11.2019

  16. Using the Bucket Method for Medical Device Risk Management w/ Mike Drues

    Opublikowany: 7.11.2019

  17. 2016 Medical Device Regulatory Trends Year in Review

    Opublikowany: 7.11.2019

  18. How Phagenesis Is Using Regulatory Affairs as They Develop a Treatment for Dysphagia

    Opublikowany: 7.11.2019

  19. What Devicemakers Need to Know About Medical Device Reporting (MDR)

    Opublikowany: 7.11.2019

  20. An Overview of What Device Makers Need to Know About CAPA

    Opublikowany: 7.11.2019

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