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Center Overview
Welcome to Southeast Regional Research Group, "A New Evolution in Site Performance". The physicians and staff
at Southeast Regional Research Group would like to form a strong relationship with you. A partnership that is
mutually beneficial. Our collaboration will not only benefit research & development within the
pharmaceutical industry, it will benefit our patient population, the Principle Investigator and his or her
practice as a whole.
From initial contact with the pharmaceutical sponsor, to the completion of the clinical trial, you will find
that the physicians and staff at Southeast Regional Research Group will be available to you throughout the
clinical research experience, including but not limited to:
- Excellence in patient care
- Completion of all regulatory documents (which include site demographics to fit the patient population)
- Budget and Contract negotiations
- Hosting of scheduled site visits from the sponsor or CRO and their staff, to include personally escorting
all persons involved and acting as a liaison
- Maintaining all study documents onsite in our local offices
- Maintaining all study related material to include study drug, devices and lab kits
- Performing all study related ancillary services to include, but not limited to, ECG's, phlebotomy,
specimen collection, testing and storage, drug infusion, radiology services, in-house pharmacist support, and
study related home health nursing staff.
- Research Coordinators and Nursing staff

Clinical Research Experience
Southeast Regional Research Group is a service business, it exists to serve its customers including sponsors,
monitors, principle investigators, and patients alike.
Southeast Regional Research Group provides a bridge between superior medical research and technology and the
medical community including the patients we serve. This bridge provides quality medical care to our patients,
increased total profits to our principle investigators in the medical community, and high quality, accurate,
and unbiased study data for our sponsors.
Our company is dedicated to excellence, customer service, and the highest satisfaction scores attainable. We
will provide medical care that, many times, would otherwise be unobtainable to our patients and will,
therefore, see a better than 90% retention rate across all phases of study.
Our staff will be cheerful, courteous, and focused on pleasing our customers. Our customers will always be
treated with importance, warmth, and respect.
Our sponsors, clients, and vendors will be treated with loyalty, and they will find their future with us to
be fruitful.
Ethically balanced financial and emotional incentive plans will be offered to PIs, our staff, and patients
alike to foster "Team", "Excellence", and "Success".
Our mission statement: Dedicated to providing superior medical research to better the lives of all those we
serve.

Facility Description
Southeast Regional Research Group facilities are headquartered in Columbus, Georgia. We also have facilities in Savannah, Georgia and we are presently expanding into Alabama, Florida, Mississippi, Texas, South Carolina, and Kentucky. Additionally, we contract with institutions and principal investigators and provide SMO services within their existing facilities across the United States.
Columbus Facility
Our medical research site in Columbus, Georgia is a 2,600 square foot facility, centrally located in the city, within six miles of most area hospitals. We recently moved to an expanded facility with five exam rooms, a large IV infusion room with leather recliners and flat screen television, procedure rooms, phlebotomy room and a fully-equipped laboratory in June 2007. This facility has an active medical staff of physicians and clinical coordinators to manage all clinical trials. Monitors have their own private desks with internet and telephone access, or they may use our spacious conference room when it is available. Subjects are allowed privacy in our quiet consent and exam rooms. In 2006, the Columbus site had nearly 125 adult admissions into clinical trials and nearly 1,200 outpatient visits. In 2007, the Columbus site attained the status of the “leading research site in the country” for several phase 2 and phase 3 studies for the treatment of complicated gram-positive skin and skin structure infections.

Investigator Experience
Staff / Consultants / Retained Consultants / Independent Contractors:
- Karen Browne, Savannah, Georgia Regional Operations Manager
- Toni Toledo, Savannah, Georgia Clinical Research Coordinator
- Michael Schaben, Savannah, Georgia Clinical Research Coordinator
- Traci Wilson, Director of Human Resources and Corporate Finance
- Amy Wilkerson, Director of Marketing
- Jennifer Hardrick, Corporate Project Manager
- Christine Senn, Clinical Operations Manager
- Kindal Klein, Research Assistant
- Barbara Drayton, Research Assistant
- Numerous PRN coordinators and nurses

Staff Expertise
Southeast Regional Research Group is led by Dr. Joseph G. Surber and Dr. Jeffrey K. Kingsley along with Dr.
Daniel Green in our Savannah office. Drs Surber, Kingsley, and Green are each Board Certified Family
Physicians with a wide array of contact in the medical community including principle investigator
representation in all subspecialties. They have worked side by side for the past seven years in this and
other ventures. They bring to the table a balanced portfolio creating astounding leverage opportunities for
Southeast Regional Research Group.
Southeast Regional Research Group is enriched with a staff of talented and hard working individuals including
clinical research coordinators, registered nurses, certified medical assistants, pharmacists, home health
nurses, and management. They bring a combined 45 years experience in the management of medical research
protocols. In their professional careers, they have a proven track record of success. Their reputation is
immaculate and their network of research institutions and principle investigators provide a clear advantage
to our success in clinical research.

Patient Demographics
Trial Management:
We offer staffing with trained and experienced clinical research coordinators; ethically aggressive subject recruitment; internal monitoring for adherence to protocol; the production of high quality, unbiased data; and accurate data management.
Site Management:
For each medical specialty we guarantee quality assurance. This is achieved with internal auditing and monitoring, Standard Operating Procedures, and well trained and experienced staffing.
Education:
We provide training for investigators and staff including compliance with FDA and HIPPA standards, ethical considerations in the protection of human subjects in medical research, and industry standards of GCP.
Performance Benchmarks:
We assess our Principle Investigators and sites for the following performance parameters:
- Speed of budget and contract turnaround
- Adherence to protocol
- Numbers of queries
- Patient enrollment results
- Patient retention percentages

Other Information
Therapeutic Areas
- Cardiology
- Dental and Maxillofacial Surgery
- Dermatology
- Emergency Medicine
- Endocrinology
- Gastroenterology
- General Surgery
- Gerontology
- Gynecology
- Hematology
- Infectious Disease
- Internal Medicine
- Medical Devices
- Musculoskeletal
- Nephrology
- Neurology
- Obstetrics
- Oncology
- Ophthalmology
- Otolaryngology
- Pain Management
- Pediatrics
- Pharmacology
- Plastic Surgery
- Podiatry
- Psychiatry
- Psychology
- Pulmonology
- Respiratory Therapies
- Rheumatology
- Trauma Medicine
- Urology
- Vascular Diseases
- Women’s Health

Contact Information
For more information, please contact:
Dr. Joe Surber
Chief Medical Officer
Southeast Regional Research Group
5210 Armour Road, Suite 300 B
Columbus, GA 31904 USA
Phone: 1-888-737-7408 (1-888-SERRG08)
Fax: 706-320-0629
E-mail:
If you are interested in contacting this center to discuss placing a clinical trial there, please complete and send the E-mail form below. A representative from the research center will then follow up with you.
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