how SAS Clinical Data Integration can help the pharma
industry meet industry requirements. clinical our organization focused not only
on clinical Research but also on the statastical Analysis System(SAS) with strong
emphasis on practical training and projects. Many companies have made great
strides in standardizing and conforming subject data collected in clinical
trials, in order to have a more efficient and repeatable way of delivering the
data to reporting systems for statistical analysis and regulatory submission.
Typically, preparing data is made up of the following three steps:
1. Specifying the conformed data
2. Programming the conformed specification
3. Validating the written programs work as expected
clinical
data warehousing and analytics, for a complimentary one-hour that will discuss
and demonstrate one way to dramatically reduce the effort of specification and
validation, as well as remove the programming step in its entirety. The ensuing
programs are automatically generated in Oracle Life Sciences Data Hub (LSH) and
as standalone SAS. The end result is a significant increase in the productivity
of data preparation and conforming for internal use, along with runnable
programs that can be sent to regulatory authorities and partners.We will provide more informations visit my site:
Contact Details :
K.Naveen SAS Trainer
+91-9177856619 (INDIA)
001-214-347-4655 (USA)
For further details:
www.sasonlinetraining.training
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