Data Driven Decisions

SAS® Life
Science
Analytics
Framework

Solutions Platforms Services

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 What? Why? and For whom?

What does the SAS® Life Science Analytics Framework do?

The SAS Life Science Analytics Framework provides a singular analytics foundation for clinical research −
paving the way for the efficient development, execution and management of the analysis and reporting
of clinical studies through a hosted environment.

Why is the SAS® Life Science Analytics Framework important?

The SAS Life Science Analytics Framework brings clinical research groups the ability to integrate any
analytic applications into the framework to deliver the power of analytics to more roles within the
organization.
These analytic applications help to improve clinical research and speed the development of new
therapies through optimized operational activities.

For whom is SAS® Life Science Analytics Framework designed?

The SAS Life Science Analytics Framework is designed for clinical researchers, making it possible for
anyone involved in data management, data standards management, biostats, clinical operations − from
programmers to executives − to efficiently manage the transformation, analysis and reporting of clinical
trials data.

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 Challenges it can Solve

• Establish one centralized clinical information repository for all development team members.
• Drive global collaboration through intuitive, easy-to-use analytics.
• Streamline clinical research processes to quickly gain insights.
• Swiftly product audit reports.

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 Benefits

1. Expand information management :-This is end-to-end management of clinical data translates to less
time spent on operational data management activities, and more time spent on exploring, monitoring
data quality and executing advanced analytics and statistics.
2. Empower multiple roles with approachable analytics:-Opens analytic applications to knowledge
workers in areas such as pre-clinical, clinical operations and medical affairs to drive global collaboration
between internal team members, consultants, contractors and development partners.
3. Global standards and study metadata management:-The model-driven approach for CDISC
standards governance and enhanced study metadata management drive efficiency from study setup to
submission.
4. streamline and automate processes:-Lowering cost and increasing speed and efficiency in clinical
research are critical to delivering future high-value treatments.
5. Team members around the world can easily access the same version of data, thereby enhancing
collaboration, drug studies and development.
6. Individual tasks and data access can be granted based on job role and function.
7. Compliance data packages for new drug submissions are prepared efficiently.

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Comparison matrix
Thank You

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