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SAS
eyes US$100mn Indian clinical research market
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April 13, 2005
SAS announced the launch of SAS drug development 3.0.
Based on the capabilities of the SAS 9 intelligence platform, SAS drug
development provides a centralized repository that allows life sciences firms to
analyze their clinical research for regulatory submission and explore new market
opportunities, product line extensions and safety issues, all within a
controlled and secure collaborative framework designed for life sciences
research industries.
SAS drug development has been designed to meet federal regulations such as 21
CFR Part 11, good industry practices and sound business practices.
Commenting on the launch, Sudipta K Sen, MD & CEO, SAS India Pvt. Ltd. said
"Pharmaceutical companies in India are gearing to find out innovative ways to
effectively manage, analyze, and explore massive amounts of complex data, and
still minimize their time to market. SAS Drug Development provides an integrated
system for managing, analyzing, reporting and reviewing clinical research
information. The solution also allows companies to increase revenue potential,
enhance the productivity of the clinical research team and improve clinical
program investment decisions - all in an environment that facilitates regulatory
compliance."
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022-5634-9400 Ext.237 |
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rajiv.kumar@sas.com |
India Infoline
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SAS
eyes US $100MN Indian Clinical Research Market
April 13, 2005
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