SAS Clinical Acceleration Repository
Support data integrity and collaboration while streamlining the path to regulatory submission.
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Maintain data integrity through a production-ready data repository that makes validation easier.
SAS Clinical Acceleration Repository supports groups and permissions, roles and privileges, electronic signatures, version control, search and an audit trail. With ownership administration and audit history, the solution helps you maintain data integrity and compliance with industry regulatory bodies and data standards.
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Integrate large and diverse data sets via an open repository.
Easily integrate data from many locations and sources, such as electronic data capture (EDC) systems, in-house clinical data management systems (CDMS), labs and contract research organizations (CROs).
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Foster collaboration.
SAS Clinical Acceleration Repository provides a single source of truth for regulated clinical trial operations with open integration to support third-party tools. The solution promotes collaboration across trials, phases and therapeutic areas, internally and with third parties.
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Improve efficiency and speed with easy-to-use dashboards.
Based on SAS Viya, SAS Clinical Acceleration Repository provides an easy-to-use, modern user experience. When used with SAS 9.4 or Viya, you can enable programming and analytics that improve efficiency and speed the path to submission.
Key Features
Help ensure data integrity and work in a validated environment while enabling collaboration and expediting regulatory submissions.
Centralized global repository
Consolidates clinical information into a single, secure, centralized global repository.
Data tracing
Traces data pedigree back to source data.
Data security
Defines data check-in/out process, audit trails, electronic signatures, versioning and role-based privileges.
Audit trails
Lets you readily determine what audit changes were made, when and by whom, for all content stored in the repository.
Secure logins
Controls all information and research team access via secure logins.
Regulatory compliance
Enables compliance with the FDA’s Title 21 CFR Part 11 requirements, as well as other industry regulations.
CDISC compliance
Complies with CDISC and its initiatives – dataset-JSON and CDISC CORE.
MDR integration
Supports integration with medical device reporting (MDR).