Medical Device Risk and Regulations with Raymond Dromms, President, Raymond P. Solutions, Inc. and Kathi Durdon, CNY Biotech Accelerator Executive Director
This presentation will include an overview of how risk plays a prominent role in product development, research and regulatory submission and will include an overview of device classification, FDA submissions and the Risk Assessment.
Register in advance for this meeting:
After registering, you will receive a confirmation email containing information about joining the meeting.
The Society of Clinical Research Associates (SOCRA - www.SOCRA.org) accepts documentation of candidate participation in continuing education programs for re-certification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area. This program will provide 1 hour of continuing education hours. When registering, note Certificate of Attendance Need (General or SOCRA).