Proven Quality and Compliance Solutions for the Life Sciences Industry

QUMAS Regulatory, Quality and Compliance Solutions address a broad range of requirements across the Life Sciences industry, from the early clinical stages, through drug discovery and development, to manufacturing, sales and marketing, all on a single platform. QUMAS Solutions provide core Content capabilities around electronic document management, SOP management, regulatory submission mangement, eCTD management, and also core Process capabilities around CAPA management, change control, deviation management, complaints management, audit management, learning management and training.

Focusing on the regulatory requirements of Pharmaceutical, Biotechnology, Generic Drugs and API Manufacturers, Contract Research and Manufacturing, and Medical Device Organizations, QUMAS Solutions deliver proven capabilities for global regulatory compliance.