By the end of the course you will:
鈥nderstand the GMP rules and guidelines associated with the preparation, completion and archiving of documentation
鈥ppreciate the importance of maintaining a comprehensive documentation system
Who should attend:
This course is appropriate to a wide ranging audience, from QA and QC, through to production and clinical trials professionals.
鈥nderstand the GMP rules and guidelines associated with the preparation, completion and archiving of documentation
鈥ppreciate the importance of maintaining a comprehensive documentation system
Who should attend:
This course is appropriate to a wide ranging audience, from QA and QC, through to production and clinical trials professionals.
