CTMG Services for Physicians

CTMG offers a new Site Specific Contract Research Organization (SS-CRO) service to assist Clinical Investigators in managing research either in their own office, or in an inpatient hospital setting. This unique SS-CRO service has enabled our Business Associate physician investigators to conduct clinical trials without interrupting their core business of seeing patients.

Our unique cGMP-like process controls, administered under CTMG’s layered Quality Systems by CTMG personnel, enables the physician to obtain premium compensation, without any expense to their practice. In our North Carolina physician sites, CTMG personnel conduct all preparatory aspects of the study for the physician EXCEPT the actual medical procedures and interpretation, as required by 21 CFR. At sites in other states distal to CTMG, experienced senior CTMG clinical personnel are in contact with one of the physician’s designated office personnel the day before, the day of, and the day after the patient visit to ensure there is no anxiety or wasted time in completing the CTMG study visit documents. Alternatively, CTMG can provide its own employee coordinators at these distal sites.

CTMG provides the following to all Investigative sites:

  • CTMG clinical coordinators prepare all documents and obtain all data for the physician, and inform the physician (or their designated staff members) of all procedures that are required at the time of the patient visits.
  • CTMG regulatory personnel create and fill out all necessary Federal and local regulatory documents.
  • CTMG contract and finance personnel negotiate both contracts and budgets on behalf of the physician. Our sites are well compensated because of CTMG’s controlled systems that ensure trial success for the Sponsoring pharmaceutical companies.
  • As Business Associates of the physician, we are able to catalogue and store all trial data at CTMG offices, where all data is converted to digital format and stored on our servers under 21 CFR Part 11 requirements.
  • The only cost to conduct the study is the time that the physician normally sees the patient. The physicians receive a premium payment for trial participation doing what they normally do in a work day seeing patients.