Design and Validability Review

The validation of the ABC Pharmaceutical facility is to be started simultaneously with the initial conceptual design. At key stages throughout the 

Through these design review meetings, cGMP and functionality requirements have and continue to be determined for each aspect of the facility, including  

Class I Equipment and Systems systems representing processes, equipment, and areas with the highest degree of product quality and regulatory impact. For example  

Class III Equipment and Systems systems representing processes, 

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Validation project management Validation responsibilities Design and validability review... 

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