QUMAS Compliance and Quality Management Solutions address a broad range of requirements across the Life Sciences industry - from the clinical phases, through drug discovery and development, to manufacturing - all on a single platform that provides critical content and process management capabilities including
- Electronic document management
- SOP management
- Regulatory submission management
- eCTD management
- CAPA management
- Change control
- Deviation management
- Complaints management
- Audit management
- Learning management and training
"On a global basis the Quality, Regulatory Affairs, R&D, Biocompatibility, Sterilization, and Technical Services departments all use the QUMAS solution, it is now starting to also be used by the Global Engineering, Global Packaging, and IT departments."
Dawn Porter, Compliance Process Lead at Hollister Inc.
For more information on a Platform approach to the management of compliance across the lifecycle of drug discovery and manufacturing, download this webinar on Regulatory Affairs and Quality Assurance Compliance on a Single Platform