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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