• Quest Life Sciences offers a full array of Clinical Trial Services,
  • Quest Life Sciences clears the Chile – ISP audit (Nov.7th – Nov.11th, 2016) without any major or minor observations.


The trained PK/Biostatistics Team at Quest life sciences is competent and provides statistical analysis for BA/BE studies and Phase II-IV clinical trials.

Bio-stats services at Quest life sciences include the following :

Protocol writing, statistical analysis and report writing. Our Bio-stats Department is well equipped with the latest software like Win NonLin and SAS

Database Programming

  • CRF Design (paper only)
  • CRF Annotation
  • Database Programming
  • Validation Checks


  • Randomization
  • Sample size estimation
  • Trial Design Inputs
  • Statistical Analysis Plan
  • Statistical Analysis

Statistical Reporting

  • Analysis & Reporting
  • Safety (ADR) Reporting
  • Feasibility analysis
  • Uploading for EDC
  • Evaluate statistical analysis & reporting
  • Give timely responses to regulatory query

Fact Sheet

  • QLS incepted in year 2004 with a clear vision of offering services to accelerate clinical development of generics.
  • Pioneers in BA/BE and clinical phase trials.
  • Over 150 bio-analytical methods developed.
  • Over 22 successful Regulatory audits
  • Successful para IV submission done.
  • Strict adherence to quality and timelines.
  • Two clinical facilities in India
  • +30 National and International PharmaSponsor companies working with Quest.
  • US FDA, EMEA, Canada, Australia, Oman and WHO approvals.
  • Excellent volunteer database of patient population in various therapeutic areas.
  • A good and strong data base of post menopausal volunteers.