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New! QUMAS Introduces R&D Suite Complete with Integration and Services
QUMAS is making the submission process faster and easier than ever before. If your current system just can't keep pace and lacks the integration to unify content and submission management into one seamless lifecycle, the new QUMAS R&D Suite is the solution to help your company realize streamlined regulatory submissions.
The QUMAS R&D Suite assists Life Science companies in expediting the new drug application process with better quality submissions, fewer iterations and shorter review and approval cycles. By combining content management, real-time collaboration with eCTD authoring templates and submission management, we provide one integrated solution for all functional R&D areas.