ALI - Research Track: Ch 3 "Investigational Product Development and Regulation" 2026

This course will provide the learner with an understanding of the three preclinical translational research parts to MedTech product development and discuss each phase of MedTech development.  This course will also provide an overview of FDA medical device classification categories and also provide the learner with definitions for common terms used in medical device development.

Authors: Rob DiBlasi, BSRT, RRT, RRT-NPS, FAARC

**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
  • Define terms common to medical device development.
  • Recognize the focus of the product team during each phase of MedTech development.
  • Review the FDA medical device classification categories.
  • Describe the three preclinical translational research parts to MedTech product development.
Chapter Three Investigational Product Development and Regulation

This course will provide the learner with an understanding of the three preclinical translational research parts to MedTech product development and discuss each phase of MedTech development.  This course will also provide an overview of FDA medical device classification categories and also provide the learner with definitions for common terms used in medical device development.

Authors: Rob DiBlasi, BSRT, RRT, RRT-NPS, FAARC

Speaker Information
Rob DiBlasi BSRT, RRT, RRT-NPS, FAARC
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