Gulf Coast Research - Inpatient and Outpatient Phase I Through IV Clinical Trials

Gulf Coast Research is a research center specializing in inpatient and outpatient Phase I through IV clinical trials.

Our exclusive network of investigators participates in pharmaceutical, biological, and medical device product development. Providing sponsors with efficient, high-quality clinical trial results is Gulf Coast Research’s primary objective.

EXPERIENCED CLINICAL RESEARCH DEVELOPMENT COMPANY

Gulf Coast Research’s custom-designed policies and procedures and quality assurance plan ensure that sponsors receive accurate, objective and timely clinical data reporting to support their drug or device development efforts.

We are a clinical research development company with over seven years of Phase I to IV experience. Gulf Coast Research only employs health-care professionals dedicated to providing the highest quality clinical trials in the industry. Many of our employees are certified CRCs.

CENTRALIZED RESEARCH CENTER ORGANIZATIONAL STRUCTURE

The centralized research center organizational structure offers sponsor and CRO clients immediate access to several pre-qualified investigators in all therapeutic specialties that our coordinators assist in managing clinical trials

Clients receive streamlined, rapid start-up of studies due to our centralized management system of regulatory management and contract development.

PK, PD, BA, BE, DIET-SPECIFIC, COMPARATIVE AND PLACEBO-CONTROLLED PHASE I STUDIES

Gulf Coast Research has over seven years’ research experience and has conducted over 200 successful clinical trials involving just about every medical specialty.

Gulf Coast Research can perform healthy subject PK, PD, BA, BE, diet-specific, comparative and placebo-controlled Phase I studies. We also have experience with Phase I studies involving special populations and disease states.

STATE-OF-THE-ART PHASE I RESEARCH FACILITY

In January 2006, our Baton Rouge office moved into a 12,000ft² state-of-the-art Phase I research facility. We have access to over 50,000 college students in the Baton Rouge Louisiana area to assist in conducting healthy subject trials.

Our facility has the capacity to comfortably house at least 55 subjects for an extended length of time. We can do this because of our bed capacity, our dining room area, our experienced staff and our terrific facility layout, which allow subjects to relax in their choice of high-speed access computer rooms or our large recreation room.

VAST AND DIVERSE NETWORK OF CLINICAL INVESTIGATORS

Gulf Coast Research contracts with pharmaceutical companies (sponsors) and Contract Research Organizations (CROs) to recruit, coordinate and manage Phase I through Phase IV clinical trials throughout our vast and diverse network of clinical investigators in South Central Louisiana.

Our highly-efficient research center structure allows us to respond quickly to the sponsor's research needs. Our centralized management and coordination system produces streamlined and rapid study start-up.

WORKING WITH PHARMACEUTICAL COMPANIES

Gulf Coast Research works closely with study sponsors and CROs to understand all aspects of each study we contract to work on.

Gulf Coast Research also works very closely with a network of investigators to recruit, enrol and schedule volunteers to participate in the studies.

HIGH-QUALITY UNBIASED STUDY DATA

Gulf Coast Research ensures that each study follows strict GCP guidelines and adheres to study protocol in order to produce high-quality unbiased study data for our sponsors.

All GCR personnel receive training in GCP guidelines, protection of human subjects, IATA certification for laboratory processing and shipping, and company SOPs before working on any clinical trial.