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E-Learning Module: GMP - Records for Medical Devices
CompuPharma Ltd
This CompuPharma GMP Module is ideal for people who are new or existing employees of the Medical Device sector and who are required to work according to GMP. The Module outlines the fundamental rules for completing records and discusses the requirements of the most frequently encountered records. Records include Device History Records, Equipment Records and Acceptance Activity Records.
Objectives:
- Define what records are
- Describe the general rules for completing records
- Explain what a quality system is and why medical device manufacturing companies use them
- List the information that must be entered on frequently used records
- List the types of records required in a medical device manufacturing company
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.
This modules is extracted from the E-Learning Course: Advanced GMP for Medical Device Operators (Certified)
Also available
E-Learning Course: Advanced GMP for Medical Device Operators (Certified)
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