Consultants

Canopy Medical, LLC consultants have wide-ranging expertise in the regulated environment of medical products. We offer an effective approach to assist companies through the challenges of concept evaluation, product development through to regulatory approval for worldwide product launch. Our goal is to provide clients a plug and play cross-functional team that can expand and contract to adapt to a client's changing needs.

Georgiann Keyport MS, RAC, ASQ CBA

Georgiann has over 25 years of experience in the drug, biologics and medical device industry and provides services in regulatory product strategy, domestic and international submission support, label development, US, CA and EU compliance, clinical trial design, quality system development and post market requirements with practical solutions to meet worldwide regulatory requirements. Please contact Georgiann Keyport directly at 952-994-8267, or gkeyport@canopymedical.com

Debbie Barber MS

Debbie has over 10 years of experience in the medical device industry. Utilizing a background in biomechanics and engineering mechanics and cross-functional industry experience, she specializes in projects requiring an integrated clinical and technical approach. This approach is applied in key services of project management, risk management, R&D, and product development. Please contact Debbie Barber directly at 612-819-0848 or dbarber@canopymedical.com

If you send us information about your company, issue or challenge, we'll assess the information and have the appropriate partner respond immediately. Please email us at info@canopymedical.com