Our focus is implementing clinical trials in physician's practices.  We handle everything from study startup to closeout with no costs to the physician.  We provide any research-specific equipment and manage every detail of the clinical trial process.  Our goal is to empower physicians to offer better care to their patients with no risk and little burden.

We provide the following services as part of site management:

• Subject study visits
• Study/site point of contact
• Study execution
• Monitoring visits and correspondence
• Drug/device accountability
• Electronic Data Capture entry
• Query resolution
• Study closeout
• Invoicing
• Marketing and advertising
• Record archiving

• SOP development and implementation
• Study identification
• Execution of Confidentiality Disclosure Agreements
• Protocol feasibility
• Site selection process
• Contract and budget negotiation
• Regulatory and startup document completion
• IRB submission and correspondence
• Source document generation
• Site initiation
• Subject identification