FDA document control room

Thank you for your interest in the DOCUMENT CONTROL ROOM PROGRAM

The purpose of this amendment 000005 is to: To extend the closing date.

All other terms and conditions remains the same.

Questions or comments must be submitted IN WRITING to pattricia.pemberton@fda.hhs.gov or leonard.grant@fda.hhs.gov . NO PHONE CALLS WILL BE ACCEPTED.



Thank you for your interest in the DOCUMENT CONTROL ROOM PROGRAM

The purpose of this amendment 000005 is to: Incorporate a complete revision of Part E and Part F of the subject solicitation and to incoporate additional documents.

All other terms and conditions remains the same.

Questions or comments must be submitted IN WRITING to pattricia.pemberton@fda.hhs.gov or leonard.grant@fda.hhs.gov . NO PHONE CALLS WILL BE ACCEPTED.



Thank you for your interest in the DOCUMENT CONTROL ROOM PROGRAM

The purpose of this amendment 000004: is to extend the closing date.



All other terms and conditions remains the same.

Questions or comments must be submitted IN WRITING to pattricia.pemberton@fda.hhs.gov or leonard.grant@fda.hhs.gov . NO PHONE CALLS WILL BE ACCEPTED.



Thank you for your interest in the DOCUMENT CONTROL ROOM PROGRAM

The purpose of this amendment 000003: is incorprate revisions in the RFP.



All other terms and conditions remains the same.

Questions or comments must be submitted IN WRITING to pattricia.pemberton@fda.hhs.gov or leonard.grant@fda.hhs.gov . NO PHONE CALLS WILL BE ACCEPTED.



Thank you for your interest in the DOCUMENT CONTROL ROOM PROGRAM

The purpose of this amendment 000002: is to incorporate revisions and additional language in the RFP.



All other terms and conditions remains the same.

Questions or comments must be submitted IN WRITING to pattricia.pemberton@fda.hhs.gov or leonard.grant@fda.hhs.gov . NO PHONE CALLS WILL BE ACCEPTED.



Thank you for your interest in the DOCUMENT CONTROL ROOM PROGRAM

The purpose of this amendment 000001: is to amend the issue date and the closing date of the solicitation on the SF1449. Box 6, issue is date is May 27, 2008, box 8, Offer Due Date/Local time is June 27, 2008 1400 ET.



All other terms and conditions remains the same.

Questions or comments must be submitted IN WRITING to pattricia.pemberton@fda.hhs.gov or leonard.grant@fda.hhs.gov . NO PHONE CALLS WILL BE ACCEPTED.



Thank you for your interest in the DOCUMENT CONTROL ROOM PROGRAM

The purpose of this amendment is to release solicitation FDA-SOL-08-00653 for the FDA Document Control Rooms. Please be advised that information concerning a cut off date for questions and a pre-proposal conference is contained within the solicitation.



Questions or comments must be submitted IN WRITING to pattricia.pemberton@fda.hhs.gov or leonard.grant@fda.hhs.gov . NO PHONE CALLS WILL BE ACCEPTED.



Thank you for your interest in the DOCUMENT CONTROL ROOM PROGRAM

The purpose of this amendment is to state the release of the subject solicitation will be made on or about May 27 and will be made available on www.fbo.gov.



Questions or comments must be submitted IN WRITING to pattricia.pemberton@fda.hhs.gov or leonard.grant@fda.hhs.gov . NO PHONE CALLS WILL BE ACCEPTED.



Thank you for your interest in the DOCUMENT CONTROL ROOM PROGRAM

This is a PRESOLICITATION NOTICE to announce the anticipated release of the solicitation for the FDA Document Control Room, on or about May 20, 2008.



The purpose of the Document Control Room contract is to acquire services to assist various FDA centers in the drug review process of complex applications through a variety of media. The successful delivery of these objectives will enable the FDA to promote, safeguard, and enhance the public health.



FDA recognizes that no single small 8(a) contractor may be capable of providing the full range of goods and services called for under this contract. Therefore, FDA encourages, where appropriate, the teaming of contractors and vendors with strong expertise. In the event the prime 8(a) contractor teams with a non-8(a) contractor it is understood that the prime 8(a) contractor must perform 51% of the requirement.



This requirement is a total small business 8(a) set-aside. The North American Industry Classification Code is 518218.



Pursuant to FAR Parts 15 & 16.5, FDA anticipates the award of single Indefinite Delivery/Indefinite Quantity (IDIQ) hybrid contract to support the Document Control Room Program.



The solicitation will be made available on www.fbo.gov.



Questions or comments must be submitted IN WRITING to pattricia.pemberton@fda.hhs.gov or leonard.grant@fda.hhs.gov . NO PHONE CALLS WILL BE ACCEPTED.



Thank you for your interest in the DOCUMENT CONTROL ROOM PROGRAM