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