Our focus is implementing clinical trials in physician's practices and increasing access to clinical research.  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:

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
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


Biotechnology

Clinical Trials

Hightower Clinical

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