Published
12 May 2011 | By QUMAS
MyQUMAS is a user friendly solution that provides access to all QUMAS Compliance Platform capabilities in one view. It allows people to easily connect and collaborate on compliance content, processes, tasks, training and reporting from one central location.
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R&D Submission Documents Package
QUMAS offers a number of Packaged Solutions providing
pre-defined and pre-tested configurations of Document
content management or Process management for specific,
common industry problems. This Package addresses
document management requirements around documents
used in Global Regulatory Submissions, particularly CTD and
eCTD submissions. The pre-defined configuration supports
the creation, approval, and ongoing lifecycle management
of documents used in functions such as Clinical, Nonclinical,
Quality, Manufacturing, Regulatory Affairs, and Safety.
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Drug Research Drug Delivery Drug Discovery & Development
Contract Research & Services Clinical Trials Contract Research Contract Services
Automation IT & Software Laboratory Instrumentation
Inward Investment Packaging Regulatory Affairs
Drug Research Drug Delivery Drug Discovery & Development
Contract Research & Services Clinical Trials Contract Research Contract Services
Automation IT & Software Laboratory Instrumentation
Inward Investment Packaging Regulatory Affairs
