Documentation

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Documentation

Documentation

Alongside use and maintenance documents, which are supplied standard with the machines, we can also supply a Validation Protocol on customer request that is written pursuant to GMP and GAMP5 standards, originated and utilized in the pharmaceutical industry. A team of specialists works exclusively in this area to develop the functional 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 on the “Documentation” service, please fill-in the contact form.