CDG e Conferences & Workshops

Clinical and regulatory training for medical devices from Clinical Device Group.

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Nancy J Stark, PhD

  • Nancy J Stark, PhD
    Owner and president of Clinical Device Group.
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Archives

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Categories

  • 510k clearance
  • 510k Working Group
  • Adverse events and effects
  • Biological Safety
  • Budgets & Costs
  • Clinical Evaluation Reports
  • Clinical Trials
  • Device deficiency
  • European requirements
  • FDA
  • Literature Reviews
  • Monitoring
  • Part 11 Software
  • Regulatory-Medical Devices
  • Reimbursement
  • Risk Analysis Reports
  • Risk Based Monitoring
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Archives

  • January 2012
  • November 2011
  • September 2011
  • January 2011
  • December 2010
  • November 2010
  • October 2010
  • September 2010
  • August 2010
  • July 2010
  • June 2010
  • July 2009
  • January 2009
  • October 2008
  • July 2008
  • June 2008

Categories

  • 510k clearance
  • 510k Working Group
  • Adverse events and effects
  • Biological Safety
  • Budgets & Costs
  • Clinical Evaluation Reports
  • Clinical Trials
  • Device deficiency
  • European requirements
  • FDA
  • Literature Reviews
  • Monitoring
  • Part 11 Software
  • Regulatory-Medical Devices
  • Reimbursement
  • Risk Analysis Reports
  • Risk Based Monitoring