DOCUMENTATION FOR VALIDATION PACKAGE

All the machines produced by AVSystems for the Pharmaceutical Industries are designed
following the FDA recommended rules: GAMP (Good Automated Manufacturing Practice).

The whole manufacturing process, starting from design up to the commissioning on site
is performed and documented in according to the following life-cycle

Before the final Issue, the Validation Package are subject to the customer approval.
Special requirement about the documentation have to be proposed and agreed
before complete the step of the U.R.S. analysis.