Phase II– IV / PK-PD & patient studies
Quest life sciences offer a full range of clinical research services for the pharmaceutical,
biopharmaceutical and CRO industries including:
- Study Development
- Site Qualification visit
- Site Initiation visit
- Interim monitoring visit
- Site Close out visit
- Intellectual Advisory Board
- External Translational Science Specialists
- Protocol Development
- CRF Design & Distribution
- Patient Recruitment
- Final report compilation and submission to various regulators
The highly capable clinical trial team helps helps the sponsor from designing stage of
the study, successful initiation, monitoring and close out activities. We offer highly-trained
and qualified project Managers, Clinical Research Associates and clinical trial assistants having
years of monitoring experience across various therapeutic areas to execute the projects.
PK-PD and Patient Studies
At Quest life sciences, we provide excellent clinical services to conduct patient population PK
studies and clinical endpoint studies on healthy volunteers and patient population for drug development
program of our sponsors. Our huge volunteer database and tie up with major hospitals and investigators’
help us conduct patient PK studies and Clinical end point studies.
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.