ALI - Research Track: Ch 4 "Clinical Research Study Op. & Reg. Affairs: Commercial Setting" 2026

This course provides learners with an understanding of the purpose and conduct of clinical research in a commercial context, including an overview of medical technology–focused research. It also explores the role of regulatory affairs within the medical technology industry and outlines the various regulatory approval pathways for medical devices.

Authors: George Dungan, MPhil, MEd

**Please note that all programs require the participant to view the entire program prior to taking the final quiz and obtaining a course certificate.**

Seminar Information
Seminar Date:
March 02, 2026
Expiration Date:
December 31, 2026 11:55 PM
Seminar Objectives
  • State the types of medical technology commercial research.
  • Understand the unique requirements for sponsored research.
  • Describe the high-level types of regulatory approval for medical devices.
  • Understand the purpose and conduct of clinical research in a commercial context.
  • Describe the roles, responsibilities, and function of regulatory affairs in medical technology industry.
Chapter Four- Clinical Research Study Operations and Regulatory Affairs: Lessons from the Commercial Setting

This course will provide the leaner with an understanding of the purpose and conduct of clinical research in a commerical context and also provide information on the types of medical technology commercial research.  This course will dsecribe role that regulatory affairs has in the medical technology industry and decribe the types of regulatory approval for medical devices.

Authors: George Dungan, MPhil, MEd

Speaker Information
George Dungan MPhil, MEd
Individual topic purchase: Selected
American Association for Respiratory Care
Continuing Respiratory Care Education: 1.50
Products
On-Demand
Member: $40.00
Student: $40.00
Full Price: $65.00