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Steven Charlebois, PhD (Vice President of Engineering, Regenerative Medicine, MED Institute Inc.)
Location: Booth 637
Date: Tuesday, February 11
Time: 12:30 pm - 1:15 pm
Track: Tech Theater
Vault Recording: TBD
Audience Level: All
Understanding the phases of the medical device development process (discovery, prototyping, design controls, regulatory approvals, clinical studies and post market activities) is the first step in accelerating their development. Leveraging experiences and resources appropriately to stay on the critical path and having the insight on when to exit is paramount. MED Institute has over 35 years’ experience developing hundreds of Class II and III medical devices as part of a large medical device company, as a consultant to physicians, and companies of all sizes and corporate structures. We are pleased to detail MED’s dedication to providing high quality services to drive development in the current market as well as our collaboration with regulators and thought leaders to help lead future innovation.