• Rob Beck specializing in clinical data base development, clinical trials
  
  
• Kathy Simpson specializing in quality system services, Lead Auditor 13485 accredited, has over 15 years in Class III, II medical device quality positions
  
  
• Linda Lavine specializing in quality support, internal audits, ISO 13485 training, Quality System Requirement training, has over 10 years medical device experience
  
  
• Jan Hintze specializing in quality engineering, six sigma lean manufacturing, development of verification and validation plans
  
  
• Anita Grossman specializing in clinical trial support, has over 10 years clinical trial development, monitoring. Her previous 20 years were as a nurse for a Catheter Lab