MODIFICATION
A -- Medical Device Safety Communications Focus Groups
- Notice Date
- 7/13/2006
- Notice Type
- Modification
- NAICS
- 541710
— Research and Development in the Physical, Engineering, and Life Sciences
- Contracting Office
- Department of Health and Human Services, Food and Drug Administration, Office of Acquisitions and Grants Services, 5630 Fishers Lane, Room 2129, Rockville, MD, 20857-0001
- ZIP Code
- 20857-0001
- Solicitation Number
- Reference-Number-Req1018369
- Response Due
- 7/26/2006
- Archive Date
- 10/1/2006
- Point of Contact
- Robert Julia, Contract Specialist/Contractor, Phone 301-827-0688, Fax 301-827-7101, - Fred Ettehadieh, Contract Specialist , Phone 301-827-5093,
- E-Mail Address
-
robert.julia@fda.hhs.gov, fred.ettehadieh@fda.hhs.gov
- Small Business Set-Aside
- Total Small Business
- Description
- The following questions have been received and are answered. Q. My company has experience conducting focus groups of hospital patients but not specifically about medical devices. Does this mean that we would most likely lose 40 evaluation points? A. It cannot be predicted how many points lack of experience directly with medical devices will cost an offeror in the technical evaluation. Similar or related experience may generate some credit if technical reviewers find it relevant. Q. Can all six focus groups take place in the Washington DC area? A. Yes Q. Will the FDA provide the contractor with lists from which to recruit? A. No Q. Is there an incumbent? A. This is a new requirement.
- Record
- SN01088083-W 20060715/060713220357 (fbodaily.com)
- Source
-
FedBizOpps Link to This Notice
(may not be valid after Archive Date)
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