Dr. Garrett has extensive experience working with industry partner corporations. He has worked in both EPA and FDA Regulated environments. He has experience with FDA regulated OTC/Rx drugs, cosmetics, high level disinfectants/sterilants, and Class I, II, and III medical devices. He also has extensive experience with EPA registered low/intermediate level disinfectants. His core areas of industry collaboration include: 

  • Medical Device Safety, Risk Management, and Infection Control Consulting
  • Legal Consulting for Outbreaks
  • Executive Leadership Development
  • DISC Profiles and Leadership Coaching
  • Live and Recorded Webinars
  • Podcasts
  • Clinical Studies Development
  • Live Presentations for Sales/Marketing Meetings
  • Key Opinion Leader Meetings
  • Medical Writing
  • Sales Meeting Training
  • Medical Science Liaison Program Development
  • Continuing Education Workshops, Webinars, and Articles
  • Sales and Marketing Clinical Training
  • Case Studies and White Papers
  • Clinical Product Development
  • Clinical/Regulatory Strategy Planning
  • Speaking Engagements (Domestic and International)
  • Medical Affairs Consulting
  • General Customer Consultation