Course curriculum

  • 1

    Welcome to the e-course!

    • How to use this course

  • 2

    General Provisions, Quality System Requirements, Design Controls, Document Controls, Purchasing Controls

    • FDA 21 CFR 820 cGMP Overview_Lesson-01

    • FDA 21 CFR 820 CGMP Overview_Lesson-01-QUIZ

  • 3

    Identification and Traceability, Production and Process Controls, Acceptance Activities, Nonconforming Product, Corrective and Preventive Actions, Labeling and Packaging Control

    • FDA 21 CFR 820 cGMP Overview_Lesson-02

    • FDA 21 CFR 820 CGMP Overview_Lesson-02-QUIZ

  • 4

    Handling, Storage, Distribution and Installation, Records, Servicing, Statistical Techniques

    • FDA 21 CFR 820 cGMP Overview_Lesson-03

    • FDA 21 CFR 820 CGMP Overview_Lesson-03-QUIZ

  • 5

    Next steps

    • Congratulations

Learning Objectives

Upon completion of this training, students will be able to:

  • Understand the requirements of the FDA 21 CFR Part 820 Quality System Regulations

  • Understand quality system definitions, concepts, and guidelines

  • Understand the roles and responsibilities to support CGMP compliance

  • Apply CGMP principles and best practices

Course Benefits:

Exceptional value | Amazing content | On Demand

  • Eliminate travel and lodging expenses

  • Save time by attending course On Demand, anytime, anywhere, with any device

  • Communicate in real-time with your course instructor - ask questions, get clarification, and contribute your insights

  • Learn through exercises and case study

  • Receive a globally-recognized certificate for successfully completing the course

Who should attend?

  • Any individual requiring a working knowledge and understanding of FDA 21 CFR Part 820 QSR

  • Quality and Regulatory Professionals and Consultants

  • Presidents/Vice Presidents/CEOs

  • ISO Coordinators/Management Representatives

  • Engineers

  • Supervisors

  • Laboratory quality professionals

  • Accredited auditors requiring the competency to audit Quality Management Systems

FDA 21 CFR 820 cGMP | 2020 Overview


Additional products

Training On Demand™