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GMP: Introduction to Good Manufacturing Practices

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

GMP: Introduction to Good Manufacturing Practices

Millions of people rely on the pharmaceutical manufacturing industry for their products. To ensure the integrity of the industry the Food and Drug Administration (FDA) created Good Manufacturing Practices (GMPs) which are found in the Code of Federal Regulations (CFR) Title 21 Parts 210 & 211. This online training course takes viewers through the regulations.

The main course sections include General Provisions, Facilities and Equipment, Manufacturing and Labeling, and Laboratory Controls and Records. Sub-topics are contained within each section. For example, the section on General Provisions gives an overview of the responsibilities of the organization and personnel such as quality control, and notes how specific education and training requirements must be met. This course concludes with a section on GMP documentation which emphasizes the importance of documenting the manufacturing process from receipt of materials through distribution of the final product.

Watch this online course for an overview of the pharmaceutical manufacturing industry Good Manufacturing Practices.

Video on Demand   This course is in the Video On Demand format, to read about Video On Demand features click here.

  • Install on any SCORM LMS
  • Full-screen video presentation
  • Print certificate and wallet card
  • You have 60 days to complete the course
Audience

Pharmaceutical manufacturing industry employees

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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