• 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.


Quest life science is an dynamic, adept- based clinical research organization. Quest life sciences with its foot prints in the US, ASEAN, CIS countries, understand the importance of quality clinical research services. We at QLS recognize the need for providing quality clinical services that is led by experience, adhering to ICH/GCP guidelines, protocol adherence, and leadership at signicant cost advantages. We provide and wish to continually provide all our sponsors/client'sa collaborative and personalized approach to meet their regulatory requirements for their generic product study submission.

By providing clinicalBA/BE & off site trial management and monitoring, quality assurance, regulatory submissions, data management and biostatistics, we are ideally suited as a progressive partner for sponsors/client's nationally and internationally.

With an experience of conducting 400+studies for various regulated markets, a good and a robust data bank of validated bio-analytical methods for over 200 molecules and the facility being inspected and approved by various global regulatory authorities, Quest life sciences ranks among the top clinical research organizations in India. Our competenciesin planning, designing and managing clinical trials - with clients that include national and international pharmaceutical majors makes us a preferred partner of choice for clinical development. Our clinical research team employ the latest study designs in BA/BE studies, BioAnalytical, pharmacokinetic analysis, project management and QA team along with support functions help us maintain and provide quality clinical services to all our client's.

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.