DiSQ is a new qualification and validation software for pharmaceutical processes, an essential process in pharmaceutical production as it provides documented evidence that a system or process complies with GMP/FDA regulatory requirements, while endorsing the correct manufacture of products at the required quality level and with a safety guarantee.

Telstar DiSQ has been designed to facilitate project management, foster standardization, guarantee traceability, ensure compliance with Data Integrity concepts, provide real-time information on the status of the different documents, and allow electronic execution and automatic generation of queries and reports on the validation status.

The life cycle of the validation of a pharmaceutical process involves a long tedious flow of editing, approval and execution that consumes time and vast amounts of paper, in addition to the process of subsequent management of this documentation, its archiving and subsequent recovery, wasting human, economic and environmental resources. The use of database applications designed for electronic and digital management optimizes the entire validation life cycle.