Do purified water equipment manufacturers need to provide 3Q validation documents to pharmaceutical companies? Should this be done by the pharmaceutical company itself or the manufacturer?

Theoretically, the equipment manufacturer to assist the pharmaceutical company to get, but this is only for large pharmaceutical companies

Small pharmaceutical companies rely almost entirely on the equipment manufacturer

GMP information is the completeness of the degree of professionalism is a measure of a water purification equipment manufacturers are qualified the most important factors. Even more important than the ability to manufacture equipment