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GMP: Introduction to Good Manufacturing Practices

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Preview Video
Course Format
  Video On Demand
Product ID
mapigmpp_vod
Training Time ?
19 to 34 minutes
Language(s)
English
Video Format
Standard Definition
Required Plugins
None
Number of Lessons
6
Quiz Questions
15
Closed Captioning
Question Feedback
Wrong Answer Remediation
Lesson Bookmarking
Interactive Producer
Mastery Training Content Network
Original Content Producer
_Multi-Media Access, Inc. (MMAX)
Overview

Good Manufacturing Practices (GMPs) keep consumers safe and companies in compliance with the law. The pharmaceutical manufacturing industry is governed by them through the Food & Drug Administration’s (FDA) Code of Federal Regulations (CFR) Title 21 Parts 210 & 211. This health and safety training course gives an overview of these regulations.

This course teaches the importance of GMP documentation. The FDA requires documentation of each stage in the manufacturing process, from receiving materials to distributing the finished product. Viewers learn GMP documentation must show compliance with GMPs that processes were controlled and consistent, and who was responsible. The documentation must also provide follow-up on the product after distribution.

Watch this health and safety course to help ensure compliance with the CFR parts 210 & 211.

Audience

Everyone who works in the pharmaceutical manufacturing industry

Topics
The course presents the following topical areas:
  • Introduction
  • General Provisions
  • Facilities and Equipment
  • Manufacturing and Labeling
  • Laboratory Controls and Records
  • GMP Documentation

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