CONTRACTS WE HAVE WORKED ON - DOMESTIC AND MILITARY CONSULTING
US ARMY - MEDICAL RESEARCH ACQUISITION ACTIVITY
CCC has two ongoing, long-term task order contracts with the US Army Medical Department for the
Army's medical research and development activities at Fort Detrick, Maryland and other locations
(DAMD17-95-C-5021 and DAMD17-98-D-0024). The following are some of the many activities and
opportunities supported by these contracts.
US ARMY MEDICAL MATERIEL DEVELOPMENT ACTIVITY (USAMMDA)
- Assemble milestone decision review document packages as required by Department of
Defense regulations in the 5000 Series for medical products in advanced development phases.
- Perform market investigations on a worldwide basis for commercial off the shelf (COTS)
items.
- Write Requests For Proposals (RFPs) for the acquisition of supplies and services required for
the testing, evaluation, and systems integration of products.
- Provide subject matter experts in the areas of nursing, microbiology, biochemistry, biomedical engineering,
financial management, medical logistics, organizational analysis, and information management and technology.
- Accomplish life cycle cost estimates, analysis of alternatives, and independent
government cost estimates.
- Assist with the development of medical communications for combat casualty care (MC4).
- Provide biomedical engineering support for development of the armored medical evacuation
vehicle (AMEV) by the integration of a variety of technologies, COTS applications, and
other Army standard systems into the prototype vehicle.
- Support Milestone Decision Authority In-Process Review meetings by creating, assembling,
and mailing "read ahead" packages, acquiring meeting facilities, hosting meeting
participants, administratively supporting meetings, recording meeting processes and
results, and creating and processing meeting minutes.
HEADQUARTERS, US ARMY MEDICAL RESEARCH AND MATERIEL COMMAND (USAMRMC)
- For the Quality Assurance Office, provide database support services for the files
maintenance of investigational new drug applications (INDs). Also, create keyword indexes,
perform data entry, and maintain historical archives.
- For the Human Use Review and Regulatory Affairs Office provide oversight evaluation of
clinical trial protocols, the conduct of clinical trials, the documenting of results, and
the submissions of new drug applications to the Food and Drug Administration.
- For the Office of Information Management provide administrative support for the breast
cancer research program and its grants application, evaluation, awarding, management, and
financial management processes.
- For the Medical Information Systems and Services agency, provide financial analysis of
installation information management processes to quantify them and provide a basis for
them to be provided to customers on a cost reimbursable basis.
DEPARTMENT OF DEFENSE JOINT VACCINE ACQUISITION PROGRAM (JVAP) MANAGEMENT OFFICE
- Provide subject matter expert for botulism and vaccinia vaccine development processes
and actions.
- Facilitate communications and information flows between bench research scientists,
applied research scientists, resource managers, milestone decision authorities, JVAP prime
contractor (production), and acquisition and logistics personnel for vaccine development.
US ARMY MEDICAL RESEARCH INSTITUTE OF INFECTIOUS DISEASES (USAMRIID)
- Provide regulatory affairs quality assurance support for the special immunization
program.
- Write investigators brochures for clinical trials.
- Train clinical trial personnel in quality assurance procedures and functions.
- Provide assistance in complying with Good Laboratory Practice (GLP),
IAW 21CFR58
(dtd 1 April 1999), for nonclinical laboratory studies.
- Provide assistance in complying with current Good Manufacturing Practice (cGMP),
IAW 21CFR606
(dtd 1 April 1999), for the production of pilot lots of test vaccines.
- Assist with the writing, assembly, and evaluation of technical data packages.
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