Quality Standards - Ci-DMS MES Software for Pharmaceuticals


CI Precision is committed to keeping pace with the changing functional, technological and regulatory requirements of the industry.

  • We keep in close contact with our customer base and survey the marketplace before implementing new functionality.
  • We continually validate our software against new operating system and database versions so that we can support them soon after release.
  • All our products have been designed to incorporate the requirements of the principal regulatory authorities.

All operational methodologies and procedures, within our products, have been validated to demonstrate that they perform their purported functions in conformance with the principles of Good Manufacturing Practice (GMP).

We incorporated standard principles into our Quality Manual in the late 1980's whilst working closely with a number of pharmaceutical companies who were developing them. We have therefore adhered to the GAMP standards since their inception in 1991. We have also been members of The International Society for Pharmaceutical Engineering (ISPE) for many years.

Call us today on +44 (0)1722 424 100 to discuss how you can dramatically reduce time to sign off batches, save money and transform your manufacturing operations. Or email your enquiry to: sales@ciprecision.com