ClinicalRM Awarded Contract for Regulatory, Clinical and Technical Services to Support the U.S. Army Medical Materiel Development Activity (USAMMDA)
HINCKLEY, Ohio, Nov. 15, 2012 /PRNewswire/ — Clinical Research Management, Inc. (ClinicalRM), a full-service Contract Research Organization providing services for basic and applied research, clinical trials, and regulatory support, announced today it was awarded a USAMMDA contract. With this contract, ClinicalRM will provide regulatory support personnel and may also provide equipment, supplies, facilities, transportations, tools, and materials necessary to support USAMMDA’s mission. The contract award number is W81XWH-13-C-0003, and is effective for 5 years, including option renewals, as of November 1, 2012.
USAMMDA supports ongoing efforts to develop new drugs, vaccines, devices, and medical support equipment that enhance readiness, endures the provision of the highest quality medical care to the Department of Defense (DoD), and maximizes the survival of medical casualties on the battlefield.
“ClinicalRM is honored to continue the support of the important USAMMDA mission through this new contract,” said Edie Druktenis, ClinicalRM Program Manager. “Our staff is highly qualified and have proven to be a great asset to the mission over the last couple of years to move solutions forward, developing medical material to protect and sustain the warfighter.
USAMMDA is the DoD’s advanced medical materiel development activity for products designed to protect and preserve the lives of Service members.
The product managers at USAMMDA guide promising new concepts and technologies developed in the U.S. Army Medical Research and Materiel Command (USAMRMC) laboratories through advanced development and the regulatory process to obtain U.S. FDA certification. Upon FDA certification, USAMMDA works in conjunction with the U.S. Army Medical Materiel Agency (USAMMA) to develop plans for fielding medical materiel.
Founded in 1992, ClinicalRM is a full service Contract Research Organization (CRO) specializing in preclinical, and Phase I to Phase IV clinical research, clinical trial support, and product development for biologics, drugs, and devices. ClinicalRM prides itself on providing outstanding customer service and exceeding client expectations. For more information, please go to: www.clinicalrm.com
SOURCE Clinical Research Management