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Upload, store and link trial documents
with other clinical data through our FDA compliant application.
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Acceliant's Document Management module is
a regulatory compliant document management application that
enables you to upload, store, manage, and link trial documents
with other clinical data in an audited, version-controlled
manner on a central data repository. The Document Management
module is tightly integrated with other Acceliant modules
to provide trial participants a single, centralized online
library for all clinical trial documents.
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| Acceliant Document Management Benefits |
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- A regulatory compliant, permission-based document management system with versioning
and complete audit trail for easy review
- Create, view, edit, and manage clinical trial documents online, including protocols,
informed consent forms, contracts, and annual reports
- Store and view essential clinical trials documents in a secure, centralized online
environment
- Manage document workflow during the clinical process, including check in/check out,
approvals, and signatures
- Reduce the frequent review of clinical trial documents by trial managers, monitors, and
regulatory personnel to accelerate clinical trial timelines
- Cost-effective and rapid deployment, without an additional IT infrastructure investment
- Optionally link with Documentum to easily complement and leverage - not replace - your
organization's existing infrastructure and technology investment
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