PRODUCTION AND BIOSAFETY TESTING OF A RETROVIRAL VECTOR SUPERNATANTFOR GENE THERAPY OF FABRY DISEASE

 

NIH GUIDE, Volume 25, Number 12, April 19, 1996

 

RFP AVAILABLE:  NIH-NINDS-96-06

 

P.T. 34



Keywords:

  Biological Resources 

  Neurological Disorders 

 

National Institute of Neurological Disorders and Stroke

 

The National Institute of Neurological Disorders and Stroke (NINDS),

National Institutes of Health (NIH),will solicit proposals for the

production of 30 liters (10 liters each year) of high-titer

retroviral supernatant solutions under GMP conditions, biosafety

testing, and delivery for the transduction of stem and progenitor

cells for patients with Fabry disease.  Offerors are required to have

a facility that has been inspected by the FDA and is in compliance

with established current Good Manufacturing Practices (GMP) and

current Good Laboratory Practices (GLP).  Offerors must have

personnel on staff with established experience in the production of

retroviruses under GMP conditions.  It is anticipated that one

contract will be awarded for a maximum period of three years.

Payment will be on a cost-reimbursement type basis.

 

INQUIRIES

 

This is not a Request for Proposals.  Request for Proposals (RFP) No.

NIH-NINDS-96-06 was issued on April 15, 1996 with responses due

approximately forty-five days thereafter.  All responsible sources

may submit a proposal that will be considered by the Government.

Requests for the RFP must cite the RFP number and include two

self-addressed mailing labels.  Written or FAX requests may be

submitted to:

 

Raina Cervantes

Contracts Management Branch

National Institute of Neurological Disorders and Stroke

7550 Wisconsin Avenue, Room 901 - MSC 9190

Bethesda, MD  20892-9190

FAX:  (301) 402-4225

ATTN:  RFP NIH-NINDS-96-06

 

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