QSR for Medical Device Companies – Basics

QSR for Medical Device Companies - Basics

The first half of UL’s two-part eLearning program on Quality System Regulation (QSR) for manufacturers and users of finished medical devices. This program begins by covering the general provisions and requirements of QSR, and continues into key topics like design controls, document and purchasing controls, identification and traceability, and product and process controls. This collection of courses provides efficient and effective high-level instruction for QA and GMP training teams and their employees.

Courses in this Program