This 12-week series lays the foundation for translating key laboratory discoveries to clinical innovations that improve patient lives. Those who are passionate about seeing their ideas come to market and who seek a practical and efficient process for making that happen will benefit from this course. Each class, taught by experts in their specialties, will include both didactic and problem-based learning. Those who attend the series consistently will have a written project proposal ready for a panel review on the final day.
Date Session Topic
6/08/22 Course overview & Introduction to Intellectual Property
6/22/22 Research Integrity and Documentation
7/06/22 Regulatory Pathways
7/20/22 Target Product Profile: A Strategic Development Process Tool
8/03/22 Quality Risk Management & Quality Dev. through GLP-Safety
8/17/22 Translational Pathways & Manufacturing through GLP-Safety
8/31/22 Moving from Basic Research to GLP Safety Studies
9/14/22 GMP Manufacturing for Clinical Use
9/28/22 Successfully Filing for First-in-Human
10/26/22 Device Translation – Lessons Learned
11/09/22 Presentation of participant projects
Meetings Streamed Online via Zoom. Registration required.
Register at: https://cvent.me/E3AXDl?RefId=concept
Wednesday, November 9 at 4:00pm to 5:30pmVirtual Event