CDG e Conferences & Workshops

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

My Photo

Nancy J Stark, PhD

  • Nancy J Stark, PhD
    Owner and president of Clinical Device Group.
Subscribe to CDG Whitepapers by Email
Subscribe to this blog's feed

Search

Archives

  • January 2012
  • November 2011
  • September 2011
  • January 2011
  • December 2010
  • November 2010
  • October 2010
  • September 2010
  • August 2010
  • July 2010

More...

Categories

  • 510k clearance (7)
  • 510k Working Group (4)
  • Adverse events and effects (2)
  • Biological Safety (3)
  • Budgets & Costs (1)
  • Clinical Evaluation Reports (3)
  • Clinical Trials (17)
  • Device deficiency (1)
  • European requirements (5)
  • FDA (15)
  • Literature Reviews (1)
  • Monitoring (1)
  • Part 11 Software (1)
  • Regulatory-Medical Devices (4)
  • Reimbursement (1)
  • Risk Analysis Reports (1)
  • Risk Based Monitoring (1)
See More

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