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SAS® Life Science Analytics Framework 

 * Overview
 * Features List
 * Learn & Support

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SAS® LIFE SCIENCE ANALYTICS FRAMEWORK


DRIVE SPEED TO MARKET WITH MORE EFFICIENT CLINICAL TRIALS.


Request Demo




GET TO KNOW SAS® LIFE SCIENCE ANALYTICS FRAMEWORK


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ONLY SAS DELIVERS A SINGLE, OPEN, CLOUD-NATIVE STATISTICAL COMPUTING ENVIRONMENT
FOR CLINICAL RESEARCH WITH EMBEDDED ANALYTIC TOOLS, SUPPORT FOR DATA STANDARDS
AND OPTIONAL INTEGRATED ANALYTIC APPLICATIONS. OUR ANALYTIC FOUNDATION FOR
CLINICAL RESEARCH HELPS YOU MODERNIZE AND DELIVER NEW THERAPIES TO MARKET FASTER
TO IMPROVE HEALTH.





KEY FEATURES

Manage and analyze information in a collaborative platform, streamline processes
and more efficiently deliver trial results to regulatory authorities.

View Features List

Read product brief



FASTER TIME TO MARKET & COST CONTAINMENT

Provides cloud-native, single solution for clinical analysis and submission with
everything you need for validation, regulatory compliance, versioning, audit
trails and documentation support. Allows for automation through workflows,
support for current and future integrations, and implements and properly manages
data standards and controlled terminology.





BROADER ACCESS TO PROGRAMMING TALENT

Gives users the flexibility to program in SAS, R and Python.





SOLID FRAMEWORK FOR TRADITIONAL & EMERGING TRIAL DESIGNS

Supports new, decentralized and hybrid trial models, including automation,
decision support and activity tracking.


IMPROVED EFFICIENCY & REDUCED ERRORS IN DATA AGGREGATION & PREPARATION

Includes central hub for all incoming data, automated data quality analysis,
better data management and analytical data preparation. Provides impact analysis
for every job and full mapping of data source, data manipulations and a final
destination for data. Includes advanced search functionality to improve
discoverability and productivity.





RIGOROUS STATISTICAL ANALYSIS & REGULATORY CONTROLS

Combines regulatory compliance and control features with seamless development
and execution of SAS programs to reduce risk.


MAXIMUM VALUE FROM EXISTING OR NEW ANALYTICS APPLICATIONS

Integrates analytic applications – including those you have already developed or
from SAS – for a variety of business needs. Ability to pull data directly from
existing EDC systems for quicker access to data and potential cost savings.





EXPANDED ACCESS TO & COLLABORATION WITH CLINICAL DATA

Includes a centralized shared workspace, clinical data repository and analytics
platform providing access for all authorized global team members. Everyone works
within the single platform.






EFFICIENTLY TRANSFORM, ANALYZE AND REPORT ON CLINICAL TRIAL DATA. DEVELOP NEW
THERAPIES FASTER BY GIVING EVERYONE ACCESS TO POWERFUL PHARMA ANALYTICS.




EMPOWER ALL STAKEHOLDERS WITH APPROACHABLE ANALYTICS.

Drive global collaboration among internal team members, consultants, contractors
and development partners by putting easy-to-use pharma analytics in the hands of
knowledge workers in areas such as preclinical operations, clinical operations
and medical affairs.




INCREASE FLEXIBILITY WITH SEAMLESS, OPEN SOURCE INTEGRATION.

Your hiring managers need the ability to hire the best programming talent
available. SAS Life Science Analytics Framework fully embraces open source,
enabling you to expand your hiring pool by giving users the flexibility to
program in SAS, R or Python. Programmers are able to consume R data frames
inside the solution.





STREAMLINE AND AUTOMATE CLINICAL RESEARCH PROCESSES TO GAIN INSTANT INSIGHT.

Workflow capabilities aid project management oversight and support process
enablement to lower costs while increasing the speed and efficiency of clinical
research. The framework supports multiple analyses with different team members,
access rights and context-specific privileges. You can assign tasks and track
progress for each analysis activity and deliverable for a single study or your
entire portfolio. Easily deploy workflows on a per-deliverable basis, whether it
be a table, listing or figure. And automate clinical process activities using
process orchestration capabilities, such as scheduled job initiation and
completion notification.




BUILD CONFIDENCE AND TRUST WITH SAS' PROVEN EXPERIENCE.

SAS is widely accepted as the gold standard for providing statistical
capabilities to determine the safety and efficacy of medicines in clinical
research. The model-driven approach for CDISC standards governance and enhanced
study metadata management drive efficiency from study setup to submission.





EXPAND INFORMATION MANAGEMENT.

A fully integrated environment spans from operational data systems (such as
eCRF), electronic health records, sensors and wearables, omics data, biomarker
data, etc., through standardization, analysis and reporting, and post-approval
meta-analysis. End-to-end management of clinical data means less time spent on
operational data management activities and more time spent on exploring,
monitoring data quality, and executing advanced analytics and statistics.




EXPLORE MORE ON SAS® LIFE SCIENCE ANALYTICS FRAMEWORK & BEYOND



Insights


ANALYTICS INSIGHTS

Get the latest news, views and best practices on analytics from the brightest
minds in the business.

Get insights


White Paper


DECENTRALIZED CLINICAL TRIALS: FROM EVOLUTION TO REVOLUTION

Examine how the COVID-19 pandemic and other events set the stage for disruption
in clinical trials, and explore the current paradigm for decentralized clinical
trials with an eye on what the future might hold for a broader revolution.

Get white paper


CUSTOMER STORY


SANTEN

Find out how Santen uses cloud-based analytics from SAS to help develop new
ocular therapies faster.

Read story


View more resources



RELATED OFFERINGS

Check out these products and solutions related to SAS Life Science Analytics
Framework.

 * Managed Application ServicesTake advantage of cutting-edge SAS technology
   with maximum uptime using managed application services from SAS.
 * SAS for Transforming Clinical Trial Analysis & Submission | Powered by
   AzureAdvance clinical data science with regulatory-grade analytics in support
   of decentralized, patient-centric clinical trials.

 * SAS® Clinical Enrollment SimulationBuild and evaluate faster, more strategic
   enrollment plans using simulation.
 * Software as a ServiceGet uninterrupted access to the specific software you
   need to make fast, accurate business decisions that deliver tangible results.

Browse all our life sciences solutions


CONNECT WITH SAS AND SEE WHAT WE CAN DO FOR YOU.


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