1359 Jaksot

  1. Compliance 360° Part 4: How To Better Manage Your Quality Data

    Julkaistiin: 27.2.2017
  2. Podcast: Brexit – Next Steps For The UK Medtech Industry.

    Julkaistiin: 27.2.2017
  3. Podcast: Attorney Discusses Cybersecurity Whistleblower Protections in Medtech

    Julkaistiin: 24.2.2017
  4. Device Week Podcast - Episode 82

    Julkaistiin: 24.2.2017
  5. Compliance 360 Part 3: Building Trust With US FDA – Can It Be Done?

    Julkaistiin: 20.2.2017
  6. Device Week Podcast - Episode 81

    Julkaistiin: 17.2.2017
  7. Compliance 360 Part 2: Getting The Most Out Of Inspection Close-Out Meetings

    Julkaistiin: 13.2.2017
  8. Device Week Podcast - Episode 80

    Julkaistiin: 10.2.2017
  9. Podcast: Mark McClellan on the Launch of the Duke-Margolis Center for Health Policy

    Julkaistiin: 10.2.2017
  10. Podcast: A Biosimilars Interview with FDA's Leah Christl

    Julkaistiin: 8.2.2017
  11. Compliance 360 Part 1: Handling Difficult US FDA Investigators

    Julkaistiin: 6.2.2017
  12. Podcast: A Conversation With Former FDA Commissioner Robert Califf

    Julkaistiin: 3.2.2017
  13. Device Week Podcast - Episode 79

    Julkaistiin: 3.2.2017
  14. Podcast: FDA’s Inspection ‘Program Alignment,’ New Guidance Docs Top QA/RA Hotspots In 2017

    Julkaistiin: 1.2.2017
  15. Device Week Podcast - Episode 78

    Julkaistiin: 27.1.2017
  16. Spinraza: A Model Approval

    Julkaistiin: 25.1.2017
  17. Podcast: 2017 Starts With New EU Regulations Imminent But Much Regulatory Uncertainty Too

    Julkaistiin: 20.1.2017
  18. Podcast: AdvaMed Discusses Aspirations For 2017, FDA

    Julkaistiin: 19.1.2017
  19. Podcast: Silicon Valley's FDA

    Julkaistiin: 18.1.2017

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Citeline places biopharma and medical device professionals, and those who focus on these industries, at the forefront of knowledge and insight, by providing the perfect combination of news and information together with penetrating insight and analysis. Citeline is a leader in the field of healthcare industry information.

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