SAS® Drug Development
Manage and share accurate clinical research information to drive informed business decisions
SAS Drug Development enables the efficient development, execution and management of analysis and reporting activities for clinical research. The solution is the only clinical repository that provides seamless integration with the SAS program development and execution environment, along with workflow capabilities that streamline processes and ease project management for analysis and reporting.
Benefits
- Global access to a single version of the truth.
- Full compliance and control.
- Streamlined processes.
- More confidence in clinical research program decisions.
- Automated integrity, traceability and transparency.
- Shorter development cycles.
" The power to get to know your compound better by using SAS Drug Development will translate into improved earnings through shorter time to market and decreased development costs."
—Stefan Driessen
Director of Global Biometrics, Solvay Pharmaceuticals
Solvay Pharmaceuticals
Screenshot
The Content repository view shows the navigation of the content repository on the left and a view of an analysis in the center section.
Screenshots
How SAS® Is Different
- SAS Drug Development provides the most seamless integration with the classic SAS programming environment available in a clinical data repository and includes all of the SAS program development and execution tools that the core user community has come to expect.
- The solution provides immediate access and ongoing insight to project progress, with better control and deployment of resources as well as the streamlining of analysis and reporting processes and tasks.
- While other solutions require extensive customization, excessive consulting expenses and protracted implementation projects, SAS Drug Development has a proven reputation for swift implementations at organizations of all sizes and can get you up and running in months, not years.
- SAS Drug Development facilitates the global collaboration that is required both within your organization and with business partners, CROs and regulatory authorities by giving clinical researchers direct access to research data, statistical results and all other relevant clinical research content via a secure, user-friendly interface, regardless of their organization or location.
- SAS Drug Development incorporates data from all relevant sources, stores all information related to a clinical research program and brings this information together in a standardized, centralized repository.
Benefits
- Global access to a single version of the truth.
- SAS Drug Development provides secure, global access to a centralized clinical information repository for all authorized development team members, so they no longer waste time and resources working on different systems across multiple organizations and geographies.
- Full compliance and control.
- The solution meets existing and emerging government regulations, including 21 CFR Part 11, good industry practices and sound business methodologies, while providing automated versioning, security, audit trails and related controls.
- Streamlined processes.
- The solution's workflow capabilities aid project management oversight and support process enablement for analysis and reporting activities by:
- Supporting multiple analyses that may have different team members and access rights and privileges.
- Providing an overall project view that gives instant insight into the status of analysis and reporting activities.
- Serving as a forum for communication between development and testing or among the entire project team.
- The solution's workflow capabilities aid project management oversight and support process enablement for analysis and reporting activities by:
- More confidence in clinical research program decisions.
- With the solution, clinical researchers can easily make critical research program decisions earlier in the process and have early visibility into trial results to enable adaptive trial designs.
- Automated integrity, traceability and transparency.
- The solution provides automated integrity, traceability and transparency documentation for all data analysis activities, which:
- Ensures ongoing quality control and assurance.
- Lets you view input data and easily reproduce your results to rapidly answer regulatory inquiries on how results were obtained.
- The solution provides automated integrity, traceability and transparency documentation for all data analysis activities, which:
- Shorter development cycles.
- The solution streamlines processes, reduces costs and speeds time-to-market by:
- Bringing together disparate information sources.
- Providing workflow functionality and seamless integration with the tools used to transform, analyze and report this information.
- Facilitating the ability to extract insights from all clinical data assets across trials, phases and therapeutic areas.
- The solution streamlines processes, reduces costs and speeds time-to-market by:
Features
- Information management
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- Consolidate clinical information into a single global repository.
- Easily review specific data set versions used, log files created, SAS programs executed and/or results generated.
- Reproduce results rapidly.
- Trace data pedigree back to the source data and rapidly answer regulatory inquiries.
- Audit changes – readily determine what changes were made, when and by whom, for all content stored in the repository.
- Compliance and control
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- Control all information within the repository via secure logins, audit trails, versioning and role-based privileges and policies.
- Quickly document the integrity of research content.
- Easily apply e-signatures when required.
- Statistical analysis
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- Integrates seamlessly with SAS programming and execution within a well-controlled and managed repository.
- Provides full control over SAS job execution.
- Loads easily and utilizes standard analytic programs.
- Allows users to check in/out new programs under development.
- Workflow
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- Assigns tasks and tracks progress for each analysis activity and each deliverable.
- Supports workflow for multiple analyses, including interim and final analyses.
- Provides flexible access rights and privileges by project.
Screenshots
The Content repository view shows the navigation of the content repository on the left and a view of an analysis in the center section.
The workflow environment shows an overview of a deliverable plus all current tasks for this user.
System Requirements
- SAS Drug Development is offered as a hosted on-demand solution.
Ready to learn more?
Call us at 1-800-727-0025 (US and Canada) or request more information.
