We can help you manage the challenges your company faces in conducting Investigator Initiated Trials (IIT).


Investigator Initiated Trials (IITs) are challenging as sponsors have to strike a delicate balance between providing oversight while maintaining a “hands-off” approach.

Exodon’s IIT division of our Product R&D department is composed of a talented group of professionals with
15 years of experience in designing and conducting IIT and post-marketing clinical research studies.

We offer comprehensive or selective CRO services from design to study close out. We can also assist the investigator by providing SOPs and GCP training, if needed, and protect the sponsor by creating a virtual firewall between sponsor and investigator.



By combining our resources and strengths, Exodon and ERA Clinical can offer the following:
       •  Study design, protocol creation, CRF development and electronic data            management
       •   Regulatory document preparation and IRB Submission
       •   Identification, selection, qualification and training of investigators
       •   Contract negotiation and management
       •   Monitor subject enrollment, and source document verification
       •   Write the FSR and assist investigator with publications, posters and             presentations

In addition, we can help you get these studies started and done in a cost effective manner with flexible payment options to meet any study budget.

To get more information or schedule a meeting click here to Contact Us

            

This program is made possible in partnership with ERA Clinical