OPERATION OF AN EXPERIMENTAL VIRUS VACCINE PRODUCTION LABORATORY NIH GUIDE, Volume 21, Number 12, March 27, 1992 RFP AVAILABLE: NIH-NIAID-DIR-93-03 P.T. 34 Keywords: Vaccine Viral Studies (Virology) Infectious Diseases/Agents National Institute of Allergy and Infectious Diseases The National Institute of Allergy and Infectious Diseases (NIAID), NIH, has a requirement for an Experimental Virus Vaccine Production Laboratory. The Division of Intramural Research, NIAID is soliciting contract proposals from organizations having the capabilities and facilities to prepare experimental virus vaccine suspensions for submission to the Center for Biologic Evaluation Research, Food and Drug Administration, using the Code of Federal Regulations (CFR), Number 21, April 1, 1990, as a guide. The viruses will include, but not be limited to: influenza, paramyxoviruses, hepatitis, rotavirus, and vaccinia viruses. The successful offeror must meet the requirements listed in the CFR for an establishment engaged in the preparation of live virus vaccines licensed for human use. The offeror will also be subject to inspection under the "Good Laboratory Practices Act" and "Good Manufacturing Practices Act." The NIAID-sponsored project will take approximately five years to complete. One contract is anticipated. This is an announcement for an anticipated Request for Proposal (RFP). RFP NIH-NIAID-DIR-93-03 shall be issued on or about March 31, 1992, with a closing date tentatively set for May 29, 1992. Requests for the RFP shall be directed in writing to: Sylvia Cunningham, Contracting Officer Contract Management Branch National Institute of Allergy and Infectious Diseases Solar Building, Room 3C07 6003 Executive Boulevard Bethesda, MD 20892 To receive a copy of the RFP, supply this office with two self-addressed labels. All responsible sources may submit a proposal that will be considered. This advertisement does not commit the Government to award a contract. .
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