• 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

Clinical Data Management

Our Clinicals’ Data Management team has valuable experience working with global and domestic sponsors and renders well timed, accurate, highest standard clinical trial data, helping you to make prompt and more effective decisions with regards to the safety, tolerability and PK |PD properties of your compound.

The team has handled both paper and EDC on all standard industry platforms. Axis offers 21 CFR Part 11 compliant integrated service | stand-alone data management support on Oracle Clinical® v4.6 with RDC platform or remotely through a secure, direct-access connection to your clinical data management system.

Our services includes but not limited to:

  • Project Specific Clinical Data Management Plan
  • Customized Database Design & Development
  • Independent Double‐Data Entry
  • Design pCRF / eCRF
  • Develop CRF completion guidelines
  • Query Management
  • Medical Coding, SAE Data Reconciliation
  • Edit, Validation and Design check
  • Programming
  • Data Validation
  • Database Testing & UAT
  • Data Migration
  • Data Loading
  • Data Cleaning
  • Quality Control and Data Quality Audits
  • Database Lock and Export to SAS
  • Project Data Archival and Storage
  • Documentation CDM Report

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..

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