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E-Learning Module: Laboratory Good Manufacturing Practice (GMP)
CompuPharma Ltd
This CompuPharma Laboratory GMP Module is ideal for both new and existing employees in the Pharmaceutical Industries, who are required to work according to the regulations of 21 CFR 210 and 211, or Eudralex Volume 4. The Module explains gMP in the laboratory, from sample receipt, testing and recording of results to result approval.
This is a self paced highly visual interactive e-Learning Module, with a full audio voiceover, which can be taken online. It has a 16 question multiple choice Assessment which the Trainee can perform once they have completed the module. For the Certified option, a hard copy certificate is mailed to the Trainee, once they have achieved a score of 100% in their Assessment.
Objectives:
- Complete laboratory records correctly
- Describe the general GMP rules that apply to the laboratory
- Describe what is done with data generated through sample analysis
- Describe what is involved in sample receipt and storage
- Explain how a sample result is released from the laboratory
- Explain what the laboratory is responsible for and the purpose of GMP in the laboratory
- Outline the steps that the analyst must take to prepare for testing in terms of solution and equipment preparation
This module is extracted from the E-Learning Course: Essential Good Manufacturing Practice (GMP) for Laboratory Analysts.
Also available
E-Learning Course: Essential Good Manufacturing Practice (GMP) for Laboratory Analysts (Certified)
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