Crafting comprehensive clinical trial protocols and ensuring compliance via clinical site audits.
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We strive to partner with medical device, pharmaceutical, and biotechnology companies to achieve and maintain global compliance in the areas of quality assurance, regulatory, and clinical affairs.
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As CEO of Medpoint, Dr. David Orr and our global team of professionals work each and every day to execute the strategies and directives of our valued clients and partners. David previously spent 26 years leading engineering development, operations, and product commercialization for medical device startups and global enterprises. As a prolific innovator of applied technologies, David has delivered products in oncology, renal, ophthalmology, cardiovascular, and tissue engineering resulting in 60+ issued patents. He also serves as Adjunct Professor with Clemson University’s Department of Bioengineering. David earned a BS in Mechanical Engineering from Rose-Hulman Institute of Technology, an MBA from Purdue University’s Krannert School of Management, and a PhD in Bioengineering from Clemson University.
Gina brings over two decades of expertise in business analysis, project management, and process improvement, with a focused career spanning four years in the medical device and pharmaceutical industries. Since joining Medpoint in 2021 as a Project Coordinator, she has demonstrated a commitment to expanding her skills by pursuing a Professional Recruiting Certificate. This credential equips her to effectively manage talent acquisition needs for Medpoint and our valued clients.
Stephanie Caddell, a distinguished member of our team, brings over two decades of expertise to our organization. With a BS in Chemical Engineering and a minor in Business Administration from Clemson University, Stephanie’s career spans 20 years in quality, operations, regulatory, and environmental roles. Stephanie’s extensive industry experience includes pivotal roles in the chemical, non-wovens, medical device, and automotive sectors. As an auditor, she has demonstrated her proficiency in ISO 9001, ISO 13485, IATF 16949, ISO 14001, and ISO 14971 standards and their associated regulations, ensuring the highest levels of compliance and operational excellence. Stephanie’s commitment to quality and regulatory compliance, coupled with her diverse industry knowledge, positions her as a key asset to our team.
Marianne has spent the last 29 years in the medical device arena. She began her career as the Purchasing Manager for Quantel (previously Big Sky Laser). From there she moved onto CoorsTek, in the role as Product and Sales Manager for Medical Products. She became the Product Manager for bone grafting products for CeraMed and after that was acquired, she was promoted to Sr. Clinical Education Manager for Dentsply Friadent CeraMed. Marianne joined Medpoint in 2018 and is the Program Manager, Operations & Quality. Marianne holds a Bachelor of Arts in English with a History Minor from Montana State University.