Tips for Accelerating Your Medical Device through the Product Lifecycle
Successfully advancing new drugs and life-saving therapies to market for emerging pharma and biotech organizations, involves complex challenges throughout the product development lifecycle. 75% of medical device companies fail and may incur up to $100B in adverse quality costs associated with correcting compliance and regulatory issues.
Gain an in-depth understanding of the Clinical Evidence Generation Process
Learn successful strategies for meeting medical device regulatory requirements
Understand the importance of developing a proactive quality strategy
Gain tips for setting up emerging companies for success
President and CEO, Clinical Research Strategies
R. Michael Tuttle
IRB Chair and Chief of Endocrinology Service
Memorial Sloan Kettering Cancer Center
Associate Chief Medical Officer & IRB Chair
University of North Carolina
Director of Human Subjects Protection
MD Anderson Cancer Center
Who should watch?
This content applies to growing medical device life science companies as well as sponsors and CROs at emerging biopharma and pharma companies. It also contains relevant insight for early-stage companies, biologics, emerging biotech companies, and anyone involved at any product development stage in advancing medical devices to market.
The Society of Clinical Research Associates (SOCRA - www.SOCRA.org) accepts documentation of candidate participation in continuing education programs for recertification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area. This program offers 1 hour of CE credit.
Certificate of Attendance
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DATE: September 29, 2022
Time: 1 pm ET | 10 am PT
Duration: 1 hour