Our DNA

CEBIS India Limited is an young, vibrant and highly dynamic clinical research organization and is in complete alignment with the need of it’s customers. We at CEBIS recognize the need for providing quality clinical services that is led by expertise, experience, adhering to ICH/GCP guidelines, protocol adherence at significant cost advantages. We provide and wish to continually provide all our sponsors/client’s a collaborative and personalized approach to meet their regulatory requirements for their generic product study submission.

By providing clinical BA/BE (healthy subjects), clinical BE (PK & PD end points) & off site trial management and monitoring, quality assurance, regulatory submissions, data management and biostatistics, CEBIS is a progressive partner for it’s sponsors/client’s.

Team with an experience of conducting studies for various regulated markets, well supported by a robust data bank of validated bio-analytical methods, we aim to be among the top clinical research organizations in India. With our competencies in planning, designing and managing BA/BE studies and clinical end point studies, we aim to become a preferred partner of choice for clinical development for our

client’s. Our clinical research team follows the continuously updated study designs in BA/BE studies, Bio- Analytical, pharmacokinetic analysis, project management and QA team along with support functions

help us maintain and provide quality clinical services to all our client’s.