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E-Learning Module: GMP - Records for Finished Dose
CompuPharma Ltd
This CompuPharma GMP Module is ideal for both new and existing employees in the Pharmaceutical Industry, who are required to work according to the regulations of 21 CFR 210 and 211, or Eudralex Volume 4. The Module explains how to complete records required for Finished Dose manufacture. Records include records of materials, production records, equipment records, laboratory records, production review and distribution records.
Objectives:
- Define what records are
- Describe the general rules for completing records
- Explain what a documentation system is and why manufacturing companies use them
- List the information that must be entered on various records
- List the types of records required in a finished dose manufacturing company
This is a self paced highly visual interactive e-Learning course, 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.
This module is extracted from the E-Learning Course: Advanced GMP for Finished Dose Operators (Certified)
Also available
E-Learning Course: Advanced GMP for Finished Dose Operators (Certified)
E-Learning Course: Advanced GMP for Solid Dose Operators (Certified)
Doing Business with Estonia
E-Learning Module: Personnel and Training
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