Documentation

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Documentation

Documentation

Alongside use and maintenance documents, which are always supplied with the machines, we can also supply a validation protocol (on customer request) written pursuant to cGMP and GAMP5 standards, originated and utilized in the pharmaceutical industry. A team of experts works exclusively in this area to develop the function and design specifications of the system, as well as all the test sheets required to carry out all the tests that the system must be put through during Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT). Documents such as QP, FS, HDS, SDS, IQ/OQ Test Protocol and others are drawn up meticulously and in continuous cooperation with the customer. For further information about documentation service, please fill in the contact form.