Anyone can print a specification sheet. This page covers how a SteriPharm machine earns the numbers on its sheet, and what paperwork arrives in the crate with it.
Designed for qualification
Our machines are designed to support common GMP practices: smooth cleanable product paths, documented contact materials, accessible sampling points and controls that log what they do. Final qualification always belongs to the operating site — our job is to make that work straightforward instead of archaeological.
A protocol, not a demonstration
Each machine model passes a written factory acceptance protocol: dimensional checks on the product path, material certificate reconciliation, function runs at rated speed, alarm and interlock verification, and an open-issues list that must close before dispatch.
What every unit passes
- Weld and surface-finish inspection on product-contact parts at defined checkpoints.
- Function run of every station and interlock before crating.
- Instrument calibration check against certified references.
- Documentation review: manuals, certificates and settings cards complete before the crate closes.
Documented and traceable
Every machine leaves with its inspection record, material certificates, instrument certificates and serial-numbered parts book. Records stay retrievable by serial number for the machine’s working life. Ask for a sample documentation set with your inquiry.
