Pharmaceutical production company Takeda Ireland is deploying the QUMAS DocCompliance platform to improve document control and compliance management across its manufacturing and quality control operations.

With QUMAS DocCompliance, Takeda Ireland will automate the lifecycles of controlled documents, reducing their review and approval cycle times and ensuring audit-readiness.

"We were very impressed with the robust functionality combined with the ease of use of the QUMAS solution," said John Cooney, director of quality assurance at Takeda Ireland.

Cooney said, "A single centralised system for the control of documentation, which can be integrated into our existing IT systems, will lead to greater efficiencies and compliance for Takeda Ireland, and is seen as a key component in our Lean Transformation programme."