On-site Record Information Management

This is Amendment 1 for the subject solicitation. 

Please refer to the SF-30, Amendement 1 (Solicitation), Q&A for Solicitation Excel Sheet, and All Updated Attachments. 

Please note that Attachment H was replaced with another version removing the drop down menu from the column titled "Reference". 

The mission of the Food and Drug Administration (FDA) is to protect the health of the American public (www.fda.gov). For more than one hundred (100) years, FDA has been the international leader ensuring safe food, cosmetics, human drugs and biologics, veterinary products, medical and radiological devices, and tobacco products. As part of its mission the FDA receives records materials from a variety of public and private entities including regulated industry. Throughout FDA‘s history, records management has played a vital role in the agency’s regulation process and, ultimately, in the mission to protect public health. This allows FDA to comply with federally mandated record keeping requirements while maintaining a high level of accountability to the citizens of the United States. In order to ensure proper organization and management of records, the FDA complies with regulations set forth in the Federal Records Act, per United States Code (U.S.C.), Title 44, Chapters 29 thru 33; Title 36 Code of Federal Regulations (CFR), Chapter 12; and National Archives and Records Administration (NARA) guidance. In addition, the FDA strives towards a streamlined, 21st Century, electronic Records Information Management (RIM) environment that preserves the integrity of public records, while creating cost efficiencies that allow the agency to focus on advancing in scientific and public health efforts.

It is the FDA’s intent to award an indefinite delivery-indefinite quantity (IDIQ) contract, with a performance period of five (5) years. The Government anticipates awarding an IDIQ contract with a ceiling of $112,000,000.00 and a guaranteed minimum of $3,000.00.

(Please refer to all attachments)