Livelink ECM — Collaborative Submissions
Livelink ECM Collaborative Submissions are a comprehensive, collaborative environment for the authoring, review, approval, assembly, export, and long-term management of all regulatory documents and submissions. Combining a full document management feature set, rich metadata support, huge scalability capibilities, and a wide range of secure, collaborative business-process tools, Collaborative submissions is the premier integrated submissions environment solution.
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Livelink ECM — Contract Lifecycle Management
Do you always know where your contracts are stored? Are you aware of all the rights and obligations agreed upon in your contracts? Have you ever missed cancellation deadlines or notice options? Livelink ECM Contract Lifecycle processes relating to a contract throughout its lifecycle - from creation through fulfillment and modification to termination.
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Livelink ECM — Microsoft SharePoint
Enables organizations to capture content created in SharePoint so that it can manage in accordance with regulations and business requirements, from a centralized lifecycle management framework. Upon this foundation, organizations can develop comprehensive compliance solutions around electronic content, ensure litigation readiness and support discovery processes, and reduce the cost of ownership of existing investments.
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Livelink ECM — Records Management
Livelink ECM Records Management empowers everyone in your organization to file all corporate holdings according to organizational policies, managing the complete lifecycle of all corporate records, thereby ensuring regulatory compliance and reducing the risks associated with audit and litigation.
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Livelink ECM — Regulated Documents
Many industry sectors such as pharmaceuticals, life sciences, financial services, and government agencies are subject to strict regulations that dictate how, when, and under what circumstances electronic documents can be authored, updated, approved, published, and archived. In the race to market, regulated industries need to make compliance with regulations an integral part of their document management and control processes to reduce risk and gain competitive advantage by bringing new products to market faster.
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Livelink ECM — Quality Management System
Open Text’s Livelink ECM – Quality Management System gives life science organizations, including pharmaceutical, medical device, biotechnology, and diagnostic companies, a flexible and expandable solution to manage quality issues and initiatives. Quality Management System provides a fully integrated solution that complies with the electronic records provisions of the U.S Food and Drug Administration’s (FDA) 21 CFR Part 11, while addressing the needs for Pharmaceutical Good manufacturing Practice (21 CFR 210 and 211), biological Good Manufacturing Practice (21 CFR 600-680) and Medical Device Quality System Regulations (21 CFR 820).
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Livelink ECM — Suite for Sap Solutions
Built on a highly scalable technology foundation, the Livelink ECM suite of Sap Solutions provides a unified platform enabling organizations runnning SAP to securely manage all documents and content (including content from non-SAP sources) within a single content repository. Superior technology, exceptional integration, and global enterprise experience ensure the highest levele of scalability, the fastest return on investment, and outstanding levels of customer satisfaction.
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