FDA 21 CFR 820 CGMP | 2022 Overview

This ON DEMAND 1-hour e-course is an annual GMP Overview of the Quality System Regulations (QSR) and FDA cGMP requirements for Medical Devices. Includes a certified training Certificate of Competence. 0.1 CEUs.

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Course curriculum

    1. How to use this course

    1. FDA 21 CFR 820 cGMP Overview_Lesson-01

    2. FDA 21 CFR 820 CGMP Overview_Lesson-01-QUIZ

    1. FDA 21 CFR 820 cGMP Overview_Lesson-02

    2. FDA 21 CFR 820 CGMP Overview_Lesson-02-QUIZ

    1. FDA 21 CFR 820 cGMP Overview_Lesson-03

    2. FDA 21 CFR 820 CGMP Overview_Lesson-03-QUIZ

    1. Congratulations

About this course

  • $95.00
  • 8 lessons
  • 0 hours of video content

Learning Objectives

After completing this training, students will:

  • Understand key concepts and major requirements of the FDA 21 CFR Part 820 Quality System Regulations

  • Know roles and responsibilities to support CGMP compliance

Course Categories

Lead Auditor | Internal Auditor | Requirements | Overview

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