Biotech & Pharma

One of the challenges in the development processes in the life science industries is to manage a global process usually performed in various sites around the world while adhering to regulatory rules such as FDA CFR 21 Part 11. This challenge is met by Sciforma which provides advanced tools for the management of close loop configurative workflows incorporating a mechanism for configuration control and document management – checked in and out – with full traceability of all actions and products of the process.