ThinkTrends Software Support
ID: FDA-RFQ-75F40125Q00156Type: Solicitation
Overview

Buyer

HEALTH AND HUMAN SERVICES, DEPARTMENT OFFOOD AND DRUG ADMINISTRATIONFDA CENTER FOR DRUG EVALUATION AND RESEARCHSilver Spring, MD, 20993, USA

NAICS

Other Computer Related Services (541519)

PSC

IT AND TELECOM - BUSINESS APPLICATION SOFTWARE (PERPETUAL LICENSE SOFTWARE) (7A21)

Set Aside

No Set aside used (NONE)
Timeline
    Description

    The Department of Health and Human Services, specifically the Food and Drug Administration (FDA), is seeking proposals for the ThinkTrends Software Support contract, which focuses on providing an AI-based Optical Character Recognition (OCR) solution for extracting data from bioanalytical reports. The primary objective is to enhance the FDA's Remote Regulatory Assessment (RRA) initiatives by achieving over 90% accuracy in data extraction, thereby improving the efficiency of remote inspections and regulatory oversight. This initiative is part of the Bioresearch Monitoring Evaluation Support Tools (BEST) platform, which has been crucial for the FDA's operations during the pandemic. Interested contractors should note that the contract will span one year, and they are encouraged to contact Robert Waite at robert.waite@fda.hhs.gov for further details, as the government will not cover any costs incurred in preparing bids.

    Point(s) of Contact
    Files
    Title
    Posted
    The FDA's Request for Quote (RFQ) FDA-75F40125Q00156 seeks proposals for the support of the ThinkTrends Software, specifically targeting AI-based Optical Character Recognition (OCR) solutions for extracting data from bioanalytical reports. The contract will span one year, set as a Total Small Business set-aside under NAICS code 541519. The objective is to enhance remote inspections through the Bioresearch Monitoring Evaluation Support Tools (BEST) and Remote Regulatory Assessment (RRA) initiatives. Contractors are expected to manage project activities, maintain communication with FDA stakeholders, and deliver accurate software solutions that achieve at least 90% accuracy in data extraction. Essential tasks include project management, software integration with study data platforms, and user support. Compliance with technical and security standards is mandatory. Involvement includes meetings with various stakeholders and adherence to FDA policies throughout the project lifecycle. The FDA emphasizes the importance of ensuring the public health by enhancing data management and regulatory processes through these innovations. Overall, this RFQ illustrates the FDA’s commitment to improving the efficiency and effectiveness of its regulatory oversight through technology.
    Lifecycle
    Title
    Type
    Solicitation
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