Services & Validations

The purpose of a DQ IQ OQ PQ validation is to document and test (through the "Validation Protocol") the composition, operation and performance of the machine under examination. The validation protocol is drafted according to the GMP (Good Manufacturing Practice) and GAMP (Good Automated Manufacturing Practice) guidelines in the pharmaceutical field.

FAT. Factory acceptance test
S.A.T. acceptance test at the customer's site
Leak test (DOP test) Filters integrity test
IQ Protocol / Installation Qualification
OQ protocol / Operational qualification
Mockup execution
Atex certification / Directive 2014/34 / EU

SMEPAC test (Standardised Measurement of Equipment Particulate Airborne Concentration)