Electronic Common Technical Document (eCTD)

Location: Maryland
Posted: Aug 14, 2026
Due: Aug 18, 2026
Agency: HEALTH AND HUMAN SERVICES, DEPARTMENT OF
Type of Government: Federal
Category:
  • D - Automatic Data Processing and Telecommunication Services
Solicitation No: 7571TE26Q00184
Publication URL: To access bid details, please log in.
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Electronic Common Technical Document (eCTD)
Active
Contract Opportunity
Notice ID
7571TE26Q00184
Related Notice
Department/Ind. Agency
HEALTH AND HUMAN SERVICES, DEPARTMENT OF
Sub-tier
OFFICE OF THE ASSISTANT SECRETARY FOR FINANCIAL RESOURCES (ASFR)
General Information
  • Contract Opportunity Type: Special Notice (Original)
  • Original Published Date: Aug 14, 2026 12:28 am EDT
  • Original Response Date: Aug 18, 2026 11:00 am EDT
  • Inactive Policy: 15 days after response date
  • Original Inactive Date: Sep 02, 2026
  • Initiative:
    • None
Classification
  • Original Set Aside: No Set aside used
  • Product Service Code: DA01 - IT AND TELECOM - BUSINESS APPLICATION/APPLICATION DEVELOPMENT SUPPORT SERVICES (LABOR)
  • NAICS Code:
    • 513210 - Software Publishers
  • Place of Performance:
    Rockville , MD 20852
    USA
Description

Solicitation Number: 7571TE26Q00184



Notice Type: Notice of Intent to Sole Source



Title: Electronic Common Technical Document (eCTD)



Description:



The National Institute of Health (NIH) intends to award a sole source purchase order for National Institutes of Allergy and Infectious Diseases (NIAID), for O Electronic Common Technical Document (eCTD). The North American Industry Classification System Code (NAICS) is 513210.



Lorenz Life Sciences Group is the only responsible source known to provide the services needed.



It is NIH's intent that the proposed action may be awarded on a sole source basis to Lorenz Life Sciences Group under the authority of Federal Acquisition Regulation (FAR) Subpart 13 Simplified Acquisition Procedures.



Contractor Objectives and Tasks:



The purpose of this acquisition is to acquire Electronic Common Technical Document (eCTD) for the purpose of performing periodic System upgrades is to maintain regulatory compliance, including ensuring adherence to current industry standards and minimizing security vulnerabilities.



This includes:



• Provides Institutes and Centers (ICs) and Clinical Research Organizations (CROs) with the ability to support the assembly and management of eCTD packages, compliant with relevant regulatory and Computer System Validation (CSV) guidelines and requirements.



• Allows compilation, publishing, validation, and review of FDA mandated regulatory submissions, such as US INDs (Investigational New drug) and US DMF’s (Drug Master File).



• Provides CROs with access to the System functionality from outside NIH Intranet.



• Provide a secure document repository for the storage of Sponsor documents with role-based access controls.



• Ensures integration of the secure document repository with the eCTD compilation and publishing tool.



o eCTD Validator



o eCTD Viewer





Sole Source Justification



In accordance with FAR 13.106-1(b), Soliciting from a Single Source, Lorenz Life Sciences Group is the only organization who can provide the services needed.



This is not a solicitation, nor is a solicitation available. However, all interested organizations may submit their capability statements and qualifications which will be considered by NIH. Responses must be in writing and must be submitted electronically to Damian Hurge, Contract Specialist at Damian.Hurge@HHS.gov by 11:00 AM EST on, August 18, 2026. Proposals must include pricing information. No late responses will be accepted.



Disclaimer and Important Notes: This notice does not obligate the Government to award a contract or otherwise pay for the information provided in response. The Government reserves the right to use information provided by respondents for any purpose deemed necessary and legally appropriate. Any organization responding to this notice should ensure that its response is complete and sufficiently detailed to allow the Government to determine the organization's qualifications to perform the work. Respondents are advised that the Government is under no obligation to acknowledge receipt of the information received or provide feedback to respondents with respect to any information submitted.



Confidentiality: No proprietary, classified, confidential, or sensitive information should be included in your response. The Government reserves the right to use any non-proprietary technical information.


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Secondary Point of Contact


History
  • Aug 14, 2026 12:28 am EDTSpecial Notice (Original)
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