SOLICITATION NOTICE
B -- Phase 2 of the Study (Medical Product Surveillance Network) which is evaluating the feasbility and effectiveness of a sentinal reporting system for adverse event reporting
- Notice Date
- 5/9/2002
- Notice Type
- Solicitation Notice
- Contracting Office
- Department of Health and Human Services, Food and Drug Administration, Division of Construction and Agency Support Contracting, 5630 Fishers Lane, Room 2129, Rockville, MD, 20857-0001
- ZIP Code
- 20857-0001
- Solicitation Number
- 223-02-6003
- Response Due
- 7/18/2002
- Archive Date
- 8/2/2002
- Point of Contact
- Susan Gane, Contract Specialist, Phone (301) 827-7166, Fax (301) 827-7103, - Paul Scarborough, Contract Specialist, Phone (301) 827-7168, Fax (301) 827-7103,
- E-Mail Address
-
sgane@oc.fda.gov, pscarbor@oc.fda.gov
- Small Business Set-Aside
- Total Small Business
- Description
- The Food and Drug Administration/Center for Devices and Radiological Health uses a contractor for implementing Phase II of a pilot project, the Medical Device Surveillance Network (MedSun). The objectives of this Internet-based device-related adverse event reporting system for use by a group of user-facilities will be met by issuance of Task Orders. The objective of each task order will be to: provide ongoing support to the facilities currently in the MedSun program; recruit and train new facilities;, develop incentives for participation; develop education and training materials for the facilities concerning not only MedSun but also recognition of device-related adverse events; provide clinical and engineering personnel who will provide follow-up and quality assurance checks to the adverse event reports sent by the MedSun facilities; provide software personnel who will provide programming support for the recruitment site and the reporting sit; provide research personnel who will aid in FDA in developing, expanding and evaluating the program; and to provide general support to the program. The Request for Proposal (RFP) will only be available on the FedBizOpps web page at http://www.fedbizopps.gov/. Prospective offers are responsible for downloading the RFP and all attachments. It is the offeror?s responsibility to monitor the FedBizOpps web page for the release of the solicitation and amendments. The RFP should be available for downloading on/about fifteen (15) days after publication of this announcement. This requirement will be a small business set-aside requirement. The FDA reserves the right to award without discussions. Technical questions shall be received not later than ten (10) days after release of the RFP. Technical questions should be sent to the Contracting Officers e-mail address or fax number contained herein. The North American Industry Classification System (NAICS) Code for this requirement is 54172.
- Record
- SN00074295-W 20020511/020509213117 (fbodaily.com)
- Source
-
FedBizOpps.gov Link to This Notice
(may not be valid after Archive Date)
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