We offer a boutique style service that allows investigators to conduct clinical trials without placing additional constraints on their time
Highly Trained
Access to highly trained coordinators with excellent documentation skills
Regulatory document completion per FDA and GCP Guidelines
Aid in patient retention and recruitment
Training with site specific SOPs
Expert Management
Communication with the sponsor and monitors
Organization and maintenance of all on-site studies
IRB submission for study start up and annual renewals
Contract and budget negotiations
Invoicing