Siena Biotech has selected the Qumas Biotechnology Package to improve document control, reduce approval lifecycles of documents and SOPs, and to become eCTD ready. Siena Biotech has also selected Qumas ProcessCompliance to automate Change Control and Non-Conformance Management and drive efficiencies across both processes.
Initially, Siena Biotech is expected to roll the Qumas applications out to 30 users.
Ken Hayward, CTO at Qumas, said: With this Package, Siena Biotech is gaining access to a world class document management solution, packaged to ensure low acquisition and implementation costs for biotechnology companies.”
Goran Westerberg, head of development operations at Siena Biotech, said: We were in the market for a flexible and up-to-date system for document management and found Qumas Solutions to be the ideal fit for our organisation, allowing the system to grow with the portfolio of the company.
Federico Paoli, head of IT at Siena Biotech, said: Qumas was able to quickly map our needs and provide a solution that fits our infrastructure.