|
COMMERCE BUSINESS DAILY ISSUE OF DECEMBER 27,1999 PSA#2503DHHS/PHS/FDA/Office Of Facilities, Acquisition, And Central Services,
Division of Contracts and Program Management, HFA-512(COB), 5600
Fishers Lane, Rockville, MD 20857 R -- CODING, ENTRY, AND QUALITY CONTROL OF MANDATORY/VOLUNTARY ADVERSE
EXPERIENCE INFORMATION RELATED TO THE PERFORMANCE OF MARKETED MEDICAL
DEVICES INTO VARIOUS COMPUTER SYSTEMS SOL 223-00-6001 POC Contract
Specialist, Susan Pearlman, 301-827-7167;Contracting Officer, Paul
Scarborough, 301-827-7168 WEB: RFP 223-00-6001,
http://www.fda.gov/oc/ofacs/contracts/. E-MAIL: Susan Pearlman,
Contract Specialist, spearlma@oc.fda.gov. Correction to CBD Notice
Posted in CBDNet on December 10,1999 -- FDA Webpage Site:
www.fda.gov/oc/ofacs/contracts/ 1. The Food and Drug Administration
(FDA), has a requirement to provide services in support of the
operation and development of adverse experience information systems
that are maintained by the Center for Devices and Radiological Health
(CDRH), CDRH develops and implements national programs to protect the
public health in the fields of medical devices and radiological health.
These programs are intended to assure the safety, effectiveness, and
proper labeling of medical devices. The intent of the Request for
Proposal (RFP) is to obtain operational and developmental support for
the information systems which enable the FDA to enforce its
responsibilities to monitor the performance, safety, and effectiveness
of marketed medical devices. A working knowledge of the clinical
aspects of medical devices and the Medical Device Amendments is
necessary for the prospective contractor to understandthe nature and
scope of this effort. The solicitation will only be available on the
FDA web page at http://www.fda.gov/oc/ofacs/contracts/. Prospective
offers are responsible for downloading the solicitation and amendments.
These documents will be in portable document format (pdf). A link to
the free downloadable Adobe Acrobat Reader software will be available
at the same site. It is the offeror's responsibility to monitor the FDA
web page for the release of the solicitation and amendments. Posted
12/22/99 (W-SN410883). (0356) Loren Data Corp. http://www.ld.com (SYN# 0088 19991227\R-0012.SOL)
R - Professional, Administrative and Management Support Services Index Page
|
|