ADVISING, COLLABORATING, AND DOING THE WORK – WHATEVER YOUR LEVEL OF NEED, WE’RE HERE.
A NETWORK OF VETERAN PROFESSIONALS
IN THE AREAS OF REGULATORY SCIENCE,
GLOBAL QUALITY SYSTEMS AND CLINICAL AFFAIRS.
Canopy Regulatory is a boutique firm founded in 2004 in Minneapolis to assist medical device and pharmaceutical companies of all sizes, from entrepreneurial to large multinational firms.
We can accommodate your firm’s level of need; augment your team or provide full support to your organization’s regulated compliance activities from development through the product lifecycle.
GEORGIANN KEYPORT
FOUNDER AND SENIOR ADVISOR
Georgiann Keyport, is the founder and Senior Advisor for Canopy Regulatory Solutions Inc., with over 30 years of practical experience in developing manufacturing processes for cellular products, establishing, and maintaining pharmaceutical medical device and streamlined quality systems, and preparing medical device and pharmaceutical submissions and managing clinical trials for start-up and established companies. She has a deep, comprehensive understanding of the regulatory submission and compliance regulations, which allow her to offer creative options and solutions to meet her client’s goals. She is an architect of strategies for product development through post market compliance.
Georgiann is a R&D cell biologist by training, holding a B.S. in Biology (St. Catherine) and M.S. in Laboratory Medicine (University of MN), holds patents in biologic technology and certifications in biomedical auditing and regulatory affairs and is a Fellow in RAPs. She is an adjunct professor in Regulatory Science M.S. Program in the School in Engineering at the University of St. Thomas, providing instruction in drug, biologics, and combination products.
YOU ARE OUR PRIORITY
We offer integrated regulatory solutions to your development projects that align with your company’s business goals. The commitment to our clients and partners remains our highest priority.