SAS Clinical Acceleration Repository

Support data integrity and collaboration while streamlining the path to regulatory submission.

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.

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).

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.

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.

Metadata repository integration

Supports integration with the metadata repository.