CTMG, Inc.

CTMG, Inc. provides auditable clinical trial controls in an interlocking system with its personnel to enable private physicians to participate in clinical trials. In addition to experienced Nurse Coordinators that perform all patient visits ni the Principal Investigators Office, CTMG has contract, finance, regulatory, and physician medical staff to ensure protocol requirements are obtained wiht appropriate Quality Assurance Review. CTMG reduces Sponsor risk by pre-screening physician sites to assure the required number of patients are seen at the PI office, establishing required site-specific Standard Operating Procedures, establishing quality system review at the site, and directly handling all operational aspects of the trial. This enables the Sponsor to quickly obtain required data and documents without interrupting the Physician Investigator's office. Physicians are able to participate as Investigators without disruption to their core business, as CTMG provides all required personnel to work within the Physicians unique office system.

CTMG has assisted Private Physicians in multipel areas, and has worked with over 40 Sponsors/CROs. Through its strategic partnerships, CTMG has access to over 4,000 physicians in Eastern North Carolina and is thus able to work with high-volume Physician Practices in multiple speciality areas. CTMG is actively seeking to merge with smaller Site Management Organizations to enable deployment of the CTMG systems in other areas of the country. CTMG has a unique mix of former Sponsor Company personnel with clinical trial experience. There are full time Physicians (with Sponsor clinical trial experience), cotnract attorneys, financial and regulatory specialists, in addition to the internal support staff, that manage the support structure systems and Quality Assurance. CTMG Nurses all have clinical trial experience, and have either MSN or BSN degrees, or LPN degrees with successful passing of the ACRP CCRC examination.

CTMG, Inc. does not see patients on its premises, but has state-of-the-art-paper and electronic retrieval and storage system for all clinical trial materials. CTMG Nurse Coordinators check out Source Document, Case Report Form, and Regulatory binders as needed to bring to their physician sites. Sponsors have the option for encrypted access to their trial folders, as CTMG makes un-editable electronic copies of all paper documents.

As CTMG seeks to work with the trial-capable, private physician sites that see the highest volumes of patients, the experience level of these investigators varies greatly. However, the interlocking system of process and operational controls deployed at CTMG enables even inexperienced Physicians to be the top enrollers in the country, with data reviewed by CTMG Quality Assurance prior to Sponsor monitor visits. In this system, Clinical Trial experience is not a pre-requisite for successful participation in clinical trials. CTMG's main offices and Principal Investigators are located in Eastern North Carolina, where there is a complete mix of patients ethnicity (Caucasion, African American, Native American, Oriental) as well as economic stratification. Eastern North Carolina also has one of the highest rates of smoking, heart disease, obesity, diabetes, renal disease, and stroke in the United States, enabling high patient enrollment in any of these studies without the need for advertising. CTMG utilizes central IRBs of the Sponsor's choice, exept for inpatient trials in which the local hospital IRB must be utilized.

Contact Information

CTMG, Inc.
Angie Congleton, BS, Director of Business and Finance
1800 North Greene Street
Greenville, NC 27834 USA
Phone: 252-752-8553 ext. 112
Fax: 252-752-4373
E-mail:

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