FDA Regulatory Compliance and EBS Submission Coordination

This contract requires the provider to serve as the primary liaison for FDA and EBS submissions related to medical device procurement, ensuring all bidder and manufacturer information is accurately documented and submitted to meet federal regulatory requirements. The role centers on maintaining compliance throughout the procurement lifecycle by coordinating technical documentation, verifying manufacturer credentials, and facilitating timely submissions to regulatory bodies to support the acquisition of medical devices for federal use. The work is associated with the Department of Defense under the Medical Supply Chain MD Surg FSF, with performance located in Annville, Pennsylvania, 17003-5003. The contract is classified under NAICS code 541611, indicating it involves management, scientific, and technical consulting services. It is structured as a subcontract with no set-aside designation, and responses must be submitted by August 3, 2026, following its posting on July 26, 2026. All activities must align with federal regulations governing medical device distribution and procurement processes.