Regulatory Affairs for Combination Products

Attend this virtual training course to learn about FDA's approach to regulation of combination products, the processes to streamline development of single entity, and aligning requirements between drugs and devices.

概要

This introductory virtual training course will provide learners with an overview of FDA’s approach to regulation of combination products including review of FDA’s recent guidance. Topics will cover processes to streamline and integrate development of single entity, co-packaged and cross-labeled products. Discussion will cover approaches to aligning requirements between drugs and devices and assuring successful human factors interface. Course material will address FDA’s expectation for post-marketing activities, including safety reporting and manufacturing modifications. Workshops will offer practical applications in when and how to report as a constituent product or as a combination.

学習目的

At the conclusion of this course, participants should be able to:

Compare the similarities and differences in drug and device regulations
Identify opportunities to streamline single entity compliance by integrating drug and device systems
Define risk assessment and management in the combination product environment
Identify the unique requirements of successful combination product development
Define FDA expectations of combination product applicants and how to work successfully with the agency
Determine how human factor considerations are assessed and controlled in the drug/device user interface

Digital Learning Catalog

Download

Regulatory Affairs for Combination Products

概要

何を学ぶか

参加対象

学習目的

Digital Learning Catalog

最新情報や機会を逃さないで