Engineering You Can Demonstrate

For regulated and critical projects, equipment performance alone is not enough.

The customer may also need evidence of how the system was specified, designed, manufactured, tested and commissioned.

Hydra-Clear can develop project documentation around the level of assurance required by the application.

Documentation Can Include

• Statement of Requirements
• User Requirement Specifications
• Functional Design Specifications
• Process Flow Diagrams
• P&IDs
• General Arrangements
• Equipment datasheets
• Instrument schedules
• Valve schedules
• Process calculations
• Hydraulic calculations
• Membrane projections
• Control philosophy
• Cause and effect documentation
• Inspection records
• Calibration records
• Pressure test certificates
• FAT documentation
• SAT documentation
• Commissioning records
• Operating manuals

Design Review

Documentation is developed progressively throughout the project rather than reconstructed after the equipment has already been manufactured.

This creates a traceable relationship between:

Requirement → Design → Manufacture → Testing → Commissioning

FAT

Factory Acceptance Testing can verify mechanical construction, automation, alarms, interlocks and process sequences before the system leaves our facility.

SAT

Site Acceptance Testing can then verify correct operation after installation.

Validation Support

For pharmaceutical and other regulated projects, Hydra-Clear can provide engineering information and documentation to support the customer's validation programme.

The precise validation scope is agreed during project definition.

Why Documentation Matters

If nobody can determine why a valve, instrument or treatment stage was specified five years after installation, important engineering knowledge has been lost.

Good documentation preserves design intent.

A system should not only work. You should be able to demonstrate how and why it works.

Call 0800 999 6770.