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Biometrics:
Our team works with you to ensure
that all regulatory, safety and scientific
requirements of your study are taken care
of right from the beginning of the project.
Software tools like WIN NONLIN and SAS
enable us to respond to your project needs
in a timely manner. Our team of experts
analyse, interpret and report your research
data. The team also networks with various
clinical teams for designing CRFs and
calculating the sample size required for
the project.
Our services include
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Statistical
design and analysis of bioavailability
and bioequivalence and Phase I/II/III/IV
clinical trials
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