The pharmaceutical industry enforces the highest quality standards for their products.

The cleaning and traceability constraints are taken in account at the very beginning of the projects, in order to deliver equipment according to the Norms and Directives ( CFR 211, cGMP, FDA) as well as European legislation, that fully meets our customers’ requirements and standards.

As a consequence, the design of our equipment is constantly reviewed and up-dated to give an appropriate answer to our customers’ latest issues.

The equipment are qualified both in our workshops (FAT) and at our customers’ site (SAT), according to a package of tests (IQ, OQ, PQ) previously approved by our customers.