Loren Data's SAM Daily™

SAMDAILY.US - ISSUE OF JUNE 29, 2022 SAM #7516
SOURCES SOUGHT

R -- FAERS Data Management Program Support Services

Notice Date

6/27/2022 11:51:36 AM
 

Notice Type

Sources Sought
 

NAICS

518210 — Data Processing, Hosting, and Related Services
 

Contracting Office

FDA OFFICE OF ACQ GRANT SVCS Beltsville MD 20705 USA
 

ZIP Code

20705
 

Solicitation Number

DAO6152201
 

Response Due

7/6/2022 11:00:00 AM
 

Point of Contact

Ian Weiss, Phone: (301) 796-5728, James G. Whitt, Phone: 2404027627
 

E-Mail Address

Ian.Weiss@fda.hhs.gov, james.whitt@fda.hhs.gov
(Ian.Weiss@fda.hhs.gov, james.whitt@fda.hhs.gov)
 

Small Business Set-Aside

8A 8(a) Set-Aside (FAR 19.8)
 

Description

This Request for Information (RFI)/Sources Sought is for information, planning and market research purposes only and shall not be construed as either an RFP/RFQ solicitation or obligation on the part of the Food and Drug Administration or its Centers.� The purpose of this RFI is to help the FDA understand industry best practices, technical solutions, and the market�s capability of fulfilling the FDA�s task requirements as described in this RFI.� FDA does not intend to make a selection decision or award a contract on the basis of responses nor otherwise pay for the preparation of any information submitted or FDA�s use of such information.� The information received may be used (for planning purposes) to inform the solicitation. Acknowledgment of receipt of responses will not be made, nor will respondents be notified of the outcome of the FDA's review of the information received.� Questions regarding the RFI cannot be accepted.� Additionally, the FDA does not intend to hold discussions concerning this RFI with any interested parties.� However, the FDA reserves the right to contact vendors if additional information is necessary.� The primary objectives of this requirement are data management services in support of the CDER Adverse Event Reporting System Data Management Program (CDER-DMP) include: Performing case processing of �mandatory and voluntary adverse event reports submitted to the FDA via the FLARe and FAERS systems. Performing data entry services of drug quality reports submitted to the FDA via the FAERS system. Maintain quality assurance programs for data entry process and manage coding services. Support changes in the data entry process that will lead to greater program efficiency.� For example, this may include updates to processes and software that maintain the accuracy of the data entry process.
 

Web Link

SAM.gov Permalink
(https://sam.gov/opp/47dd3ccab2614128bbd5e945c6520a51/view)
 

Place of Performance

Address: Silver Spring, MD 20901, USA

Zip Code: 20901

Country: USA
 

Record

SN06370747-F 20220629/220627230104 (samdaily.us)
 

Source

SAM.gov Link to This Notice
(may not be valid after Archive Date)

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