ABSTRACT
This master plan presents a medium in which the department concerned with completing the cleaning validation can mutually ensure regulatory compliance. The management (and/or designate) of production, quality control (chemical and microbiology), packaging, quality assurance, and validation will
Agree on the requirements of the CVMP prior to implementation• Discuss/determine the validation approach for completing each segment of the • CVMP Direct the integration and maintenance of the CVMP•
The specifi c responsibilities of departments and individuals supporting the cleaning validation are as follows.
