• AXIS Clinicals successfully completes 25th US FDA audit (November 2018)
  • AXIS Clinicals successfully completes 4th MHRA audit (June 2018)
  • AXIS Clinicals successfully completes 2nd WHO audit (December 2017)
  • AXIS Clinicals successfully completes AEMPS Spain (December 2018)
  • AXIS Clinicals successfully completes INFARMED Portugal (June 2018)
  • AXIS Clinicals successfully completes NPRA Malaysia (June 2018)
  • AXIS Clinicals successfully completes GCC audit (February 2016)
  • AXIS Clinicals successfully completes MCC South Africa audit (March 2017)
  • BA-BE studies conducted at AXIS Clinicals are accepted by Chile – ISP

PK | Biostatistics & Programming

PK | Biostatistics Team at Axis is competent and offers accurate statistical analysis for BA | BE studies and Phase II-IV clinical trials. Our diversely experienced personnel bestow intuition into trial design, develop complex statistical analysis plans and support clients throughout the regulatory filing process.

Biometrics services at AXIS Clinicals include protocol writing, statistical analysis and report writing. Our Biometrics Division is well equipped with the latest software like Win NonLin and SAS (SDMS & MED X view).

Our Biostatistics team is capable of handling amendments in Sponsor requirements and is swift to respond, striving for complete satisfaction with the best quality or timelines. Our services include:

Database Programming

  • CRF Design (paper & electronic)
  • CRF Annotation
  • Database Programming
  • Validation Checks


Data Management

  • Data Acquisition
  • Data Reconciliation
  • Discrepancy Management
  • Medical Coding (MeDRA & WHODD)
  • Database Lock
  • Data Extraction for Reporting



  • Randomization
  • Sample size estimation
  • Trial Design Inputs
  • Statistical Analysis Plan
  • Statistical Analysis
  • Biostatistics Subject Matter Expert (Tie up with global consultants)


Statistical Reporting

  • TLF Programming
  • CDISC Data Mapping (SDTM & ADaM)
  • Clinical Data Repository
  • Pooled Data Analysis & Reporting
  • Safety (ADR) Reporting
  • Patient Profiles & Data Cleaning Reporting
  • Feasibility analysis
  • Help in SAP & TLG|F mock shell preparation | CDISC | SDTM | ADaM standards
  • Uploading for EDC | Blinded envelops
  • Work on PK | PD Calculations
  • Evaluate statistical analysis & reporting
  • Provide preliminary results review
  • Give timely responses to regulatory query
  • Stay informed about the up-to-date statistical techniques approved by regulatory authorities such as USFDA, EMEA and DCGI


Fact sheet

  • 2,600+ clinical studies completed since inception
  • 350+ bioanalytical methods developed
  • 50+ successful Regulatory audits
  • Global footprint of operations with sites in India, U.S & Mexico.
  • Two clinical facilities (Hyderabad & Ahmedabad) in India
  • 100+ National and International Pharma/Biotech Sponsor companies working with AXIS
  • US FDA : 500+ approvals, EMEA : 100+ approvals, Canada : 50+ approvals, Australia : 50+ approvals
  • 500+ experienced employees working globally
  • Huge database of patient population in various therapeutic areas viz. Cardiology, Opthalmology, Schizophrenia, Diabetology, Oncology. Orthopedics etc..

Copyright Axis Clinicals - All Rights Reserved