Methodology

Pharmagraph recognises the importance of working with the customer all the way from project conception to project completion. The User Requirements Specification, Functional Specification, Design Specifications, Test Specifications and Qualification Protocols form the cornerstones of our approach. In line with the GAMP guides, we believe that the responsibility for a successful outcome is shared between Pharmagraph and the customer. With over 12 years experience in supplying computer based monitoring systems to the pharmaceutical industry, Pharmagraph embraces the latest technology to deliver 21 CFR part 11 compliant solutions that are easy to use and maintain.

Our commitment to the customer doesn’t stop at project completion; our services extend to help line support, routine calibration and maintenance, decommissioning and data migration.