Site Identification and Feasibility

We are aware that Key Investigators and Opinion Leaders are vital for your clinical research to succeed. Thus, years of experience in the domain helps us to handpick the best and the most relevant sites ideal for your study.

Clinox leverages its expert knowledge of the local affairs and existing relations with teams, investigators and site staff throughout your study.

Pre-existing relations with experienced investigators allow us to facilitate punctual yet comprehensive feasibility assessment to ascertain that the most ideal recruiting sites are chosen for the projects of our sponsors.

Review of site facility, resources, source documentation practices, EC’s SOP etc. and up-scaling (as and where required) to meet the ICH-GCP and applicable regulatory requirements (Schedule-Y).

Identification and development of potential Principal Investigator(s) (PIs)

Assistance in the execution of Undertaking by the Investigator (Appendix-VII of Schedule-Y), Form FDA 1572, Financial Disclosure, Clinical Trial Agreement etc.

Communication with study Sponsor/CRO

Translation and validation of ICF in required vernacular language(s).