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SMO-USA, Inc. |
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Center Overview
Created in 1996, we are a Site Management Organization with 3,500 affiliated experienced Principal Investigators whose sole purpose is to support the successful outcome of clinical investigations. Our goal is to earn the recognition as a company that provides our customer with unparalleled service, responsiveness and results. WE ARE NOT JUST ANOTHER SMO - JUST AS YOUR STUDY IS NOT JUST ANOTHER PROTOCOL!
We feel the cornerstone of any successful business relationship is effective communication, swift responsiveness to your needs and RESULTS.
We do not feel that "bigger is better" and continually evaluate our ability to adequately manage our existing studies before accepting additional assignments
Clinical Research Experience
We have conducted over 800 inpatient and outpatient trials in the therapeutic areas of:
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Facility Description
We are centralized for administrative, contractual, and budgetary issues to facilitate swift site identification, qualification, selection and start up across multiple sites.
We screen our database and present to the customer only the most highly qualified and experienced sites based on the Sponsor's specific criteria.
Each site has dedicated, full time, and experienced Clinical Research Coordinators to expedite regulatory and start up activities.
We utilize Central IRB's for outpatient studies and local IRB's for inpatient studies.
Each study is assigned a Project Manager who serves as a central contact for all sites to ensure efficient communication and that barriers to a successful outcome are minimized.
Investigator Experience
All investigators in our database have been screened to ensure that they are experienced clinicians and researchers. All investigators are Board Certified/Eligible in their respective therapeutic area.
Staff Expertise
Each site has dedicated and experienced Clinical Research Coordinators.
Patient Demographics
Because our investigative sites are located throughout the United States, Puerto Rico, and Canada, we have access to a myriad of patient populations.
Other Information
Benefits to using SMO-USA, Inc.:
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EFFICIENCY
Since we utilize our database to identify experienced investigators based on your specific criteria, a significant amount of time is saved during the initial site screening process.
Because of our ability to present multiple sites, one call can help you identify and select numerous qualified Investigators. You are always free to select only those sites that you want. We do not require "All Sites or No Sites".
Budgetary and contractual discussions are always centralized, thus minimizing lengthy negotiations for each site.
QUALITY
All of the Investigators in our network are highly experienced clinicians and researchers. In order to become part of our network, a physician must demonstrate that they have successfully participated in at least three, preferably five, clinical studies.
Clinical Research Coordinators must also meet stringent criteria. Since we place an enormous amount of responsibility for the success of your study with them, we ensure they have the skills and capabilities to manage it appropriately.
Contact Information
For more information, please contact:
Richard Turner
President
SMO-USA, Inc.
8014 Cumming Highway
Suite 403-346
Canton, GA 30115 USA
Phone: 770-704-8215
Fax: 770-345-9187
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.
