Essentially all of our process equipment was manufactured in the U.S., Europe or Japan.

All equipment has been validated to meet international regulatory requirements including :

  • Design Qualification (DQ)
  • Construction, Installation and Commissioning Qualification (IQ)
  • Operation Qualification (OQ) • Performance and Process Qualification (PQ)
  • On-going validation maintenance will be documented using the SAP Enterprise Resource Planning (ERP) Information Systems module dedicated to this function

Validation Master Plan (.pdf)

Automation Systems at ScinoPharm (.pdf)

At the ScinoPharm facility in Tainan, there are many HART (Highway Addressable Remote Transducer) instruments that manage process equipment and utility control functions. These are controlled using the Fisher Rosemont Delta V process automation system.