Site Management Support

Our dedicated team of professionals at Clinox, focus and commit themselves to ensure quality deliverables. With our extensive experience in the domain, we extend complete site management support to ensure a smooth start-up planning for you.

Clinox leverages its pre-existing agreements with several sites who have expert investigators, reliable infrastructure with essential facilities that are required for clinical trials. Thus, we assist with the selection of the most trusted investigator sites with the help of our structured feasibility.

An overall support throughout your trial, in the best way possible, is what you can expect from Clinox.

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).