To ensure the success of your clinical trial, it is important to have an experienced, appropriately trained, and qualified team. Our monitors are committed to development and implementation of enrolment strategy, and ensuring compliance of trial site with study protocol, GCP and applicable regulatory requirements. Our Team manages the collection and processing of all regulatory documents, obtaining IRBs approvals (Local Ethics Committee), site GCP, and responds to all Corrective And Preventive Action (CAPA) plans and query resolution.
Identifying the right clinical trial sites for the study is the first and very important step each clinical trial. The right site is not only the site that has access to patient population and experience in clinical trials, but also the site which will be committed to your clinical trial. Our sites have been pre-screened by our staff to be in compliance with GCP with high professional and ethical standards. Our clinical site reach includes the US, UK, France, Netherlands, Sweden, Serbia, Croatia, Slovenia, Bosnia and Herzegovina, Montenegro, Macedonia, and Hungary.
1038 Jaeger Street Columbus, OH 43206