We offer a wide range of data analytics services in different therapeutic areas. Our Ph.D. trained biostatistics team with strong methodological expertise will work with you to design your study with appropriate primary and second endpoints, develop data collection and analytical plans, and analyze the data to produce statistical reports. During the protocol development stage, our team will help to understand different scenarios and assumptions to finalize the sample size calculations and study endpoints. We are also well versed with the regulatory requirements for data reporting and provide data conformance for NME/IND submissions.

We specialize in the following services:

• Clinical Trails Design

• Randomization Plans

• Drafting of Statistical Analysis Plans (SAPs)

• Sample Size Calculation

• Data Collections

• Clinical Data Management

• Data Analysis

• eCRF Review

• Data Conformance for NME/IND submissions

• SAS, R, STATA, PRISM

• Production of Statistical Reports (Phase I-IV)