We pay attention to regulatory changes.

As validation requirements have evolved, so has our approach to validation.

As a project takes shape, documentation needs are addressed at the earliest stages.

The incremental review of key documents during the design and construction process opens lines of communication with the customer to prevent problematical and costly modifications in the final project stages.

Custom Powder Systems completed Installation Qualification (IQ) and Operational Qualification (OQ) documentation and validation packages provide documented evidence that our systems are built and commissioned in accordance with user requirements (URS), functional specifications (FS), and FDA and cGMP standards.

Functional Acceptance Test