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clinicaldevice

  1. Choosing A Device CRO-Consultancy bit.ly/Hd035n 8:52 AM Apr 3rd via TypePad
  2. A Strategic Approach to Protocol Design bit.ly/zPzWQR 3:31 PM Mar 13th via TypePad
  3. Uptick in Clinical Evaluations bit.ly/yY1WDF 11:10 AM Feb 21st via TypePad
  4. Deviations and Amendments bit.ly/AxUy7W 3:59 PM Feb 1st via TypePad
  5. Deviations and Amendments Workshop bit.ly/AxUy7W 3:56 PM Feb 1st via TypePad
  6. Adverse Event Reporting for Medical Device Trials bit.ly/zs3iqS 4:51 PM Jan 31st via TypePad
  7. Device AEs Exceed Drug AEs in 2008 bit.ly/w4ccfT 4:32 PM Jan 31st via TypePad
  8. Good Monitoring Practices—"Good Grief! What Now?" bit.ly/aSMITg 4:13 PM Jan 31st via TypePad
  9. Introduction to Medical Device Regulation: US bit.ly/x9Y156 3:25 PM Jan 31st via TypePad
  10. Introduction to Medical Device Regulation: US bit.ly/acP8XM 3:22 PM Jan 31st via TypePad
  11. Relationship Building in Clinical Trials bit.ly/AEJqL7 1:58 PM Jan 22nd via TypePad
  12. Relationship Building in Clinical Trials bit.ly/AEJqL7 11:21 AM Jan 20th via TypePad
  13. Risk-Based Monitoring—The New FDA Guidance bit.ly/w5g7p9 8:23 AM Dec 6th, 2011 via TypePad
  14. Risk-Based Monitoring for Device Trials bit.ly/sYZcOO 1:52 PM Nov 22nd, 2011 via TypePad
  15. Risk-Based Monitoring—The New FDA Guidance bit.ly/w5g7p9 1:06 PM Nov 13th, 2011 via TypePad
  16. Risk-Based Monitoring—The New FDA Guidance bit.ly/vX6310 12:50 PM Nov 13th, 2011 via TypePad
  17. How to Write A Clinical Evaluation bit.ly/pWUdPM 4:41 PM Sep 25th, 2011 via TypePad
  18. Literature Evaluations for Biological Safety bit.ly/r3OUBM 2:32 PM Sep 25th, 2011 via TypePad
  19. Clinical Trial Agreements bit.ly/r8gYmt 12:22 PM Sep 1st, 2011 via TypePad
  20. Registry Studies: Why and How http://bit.ly/qCoOzq 5:33 PM Jul 19th, 2011 via TypePad