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Documentation is the cornerstone of any company’s quality management system and is an essential GMP requirement. It is critical that anyone dealing with GMP documents and documentation systems understand the regulatory requirements and adopts best practice. As such this course provides a step by step explanation of what to do when managing GMP documentation and documentation systems.
Suitability
This course is appropriate to a wide ranging audience, from QA and QC, through to production and clinical trials professionals.
By the end of the course you will:
Understand the GMP rules and guidelines associated with the preparation, completion and archiving of documentation
Appreciate the importance of maintaining a comprehensive documentation system
