PK-PD & patient end point studies

CEBIS team supports the sponsor from designing stage of the study, successful initiation, monitoring and close out activities. We offer qualified Clinical Research Associates and clinical trial assistants having years of monitoring experience across various therapeutic areas to execute the projects.

At CEBIS, we offer services to conduct patient population PK studies and clinical endpoint studies on healthy volunteers and patient population. Our tie up with major hospitals and investigators’ (through experienced SMO) help us conduct patient PK studies and Clinical end point studies.

The following services are offered by CEBIS :

• Protocol Development
• CRF/ICF Design & Distribution
• Site Qualification visit
• Site Initiation visit
• Patient recruitment
• Interim monitoring visit
• Site Close out visit
• PK/stats and eCTD CSR