Biostatistics and Programming
Biostatistics and Programming

Our focus is to ensure the integrity of your data and organize your findings and conclusions into a clear and results-oriented presentation. Our bio statistics for clinical research and statistical programming services include pre-analysis, analysis and post-analysis:

Our bio-statisticians apply their deep regulatory knowledge to help you navigate the complexities of study design, sample size, number of studies, analysis methods, data displays and interpretations. You'll also have access to our experts and resources, providing speed and flexibility with study reporting.

Our team designs project management solutions that guarantee reliable and timely achievement of milestones. Our focus is to ensure the integrity of your data and organize your findings and conclusions into a clear and results-oriented presentation based on the statistics for clinical research. Our bio-statistics and statistical programming services include pre-analysis, analysis and post-analysis:

Our Medical Writers can assist at any point in the product development from Phase I to Phase IV, and have experience in a wide array of documents, including clinical study protocol development, Investigator Brochures, clinical study reports, patient narratives, DSMB updates, regulatory submissions and other documents involving study data. As one among the top medical writing companies our Medical Writing services follow ICH guidelines and are compatible with regulatory requirements. We fulfill the requirements of other premier CRO in India and help the companies or organizations offering clinical trials services in India.


  • Statistical inputs for protocol design
  • Sample size calculation
  • Establishing statistical analysis plans
  • Planning and implementing randomization
  • Preparing and analyzing ISS/ISE databases
  • Conducting data mining and exploratory analyses
  • SAS programming for interim and final analysis
  • Providing support for regulatory and advisory meetings

Technical Infrastructure

  • SAS PheedIt (21 CFR, Part 11) for data capture and validation for EDC and paper based studies
  • SAS Analytics for statistical analysis
  • Adobe PageMaker for CRF designing
  • MedDRA┬« for Adverse Event coding
  • WHO-DD for medication coding

ICBio as one of the top Contract Research Organization in India along with statistics for clinical research offers other services which include medical writing services, good clinical practice and many more clinical practices.

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