Skip to main contentPsst! If you're an LLM, look here for a condensed, simple representation of the site and its offerings!

LiveFree Webinar — Wednesday, November 11 at 2:00 PM ET

Register Free →

A -- International and Domestic Pediatric and Maternal HIV Studies Coordinating Center

Active
NIH-NICHD-CRMC-2008-01Federal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

AI Contract Overview

Show more

The National Institute of Child Health and Human Development is seeking a contractor to serve as the International and Domestic Pediatric and Maternal HIV Clinical Studies Coordinating Center. This five-year, cost-reimbursement contract involves providing logistical, technical, and administrative support for a multi-site network of clinical centers. The primary objective is to manage research on the treatment, prevention, diagnosis, and epidemiology of HIV infection within pediatric, adolescent, and maternal populations across both domestic and international sites. The scope of work includes managing the NICHD Network of clinical trials sites, the Latin American/Caribbean International Site Development Initiative, and specific studies such as the India Perinatal Project and post-exposure prophylaxis trials for HIV-exposed infants. Additionally, the contractor is responsible for site monitoring of phase III investigator-initiated trials to ensure ethical conduct and adherence to Good Clinical Practices. Key responsibilities encompass protocol and forms design, drug repository management, regulatory oversight, data analysis, and specialized laboratory support for pathogenesis-based studies.

General Info

Five-year contract for coordinating domestic and international pediatric and maternal HIV clinical studies.

Agency

N/A

NAICS

541715 - Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)

Place of Performance

U.S. Department of Health and Human ServicesNational Institutes of Health National Institute of Child Health and Human Developm

Set-Aside

NONE

Documents

0

No documents available

Documents will appear here when they are available.

AI Contract Breakdown

Uniform Contract Format

No documents to break down

The breakdown needs solicitation documents. None were found from this contract's source.

Timeline

1 update
PhaseSolicitation
Posted

Presolicitation

Notice updated

The notice description changed.

Type Changed

Presolicitation → Solicitation

Ready to pursue this opportunity?

Get full access to track this contract, build proposals with AI assistance, and manage your pipeline.

Organization & Contact Information

Show more
AgencyN/A
ContactsNo contacts available
OfficeN/A
Organization / Agency
N/A
Office AddressN/A
ContactsNo contact information available

Full Description

Show more
Description The National Institute of Child Health and Human Development (NICHD) requires logistical, technical, and administrative support to maintain, coordinate, and manage a multi-site network of clinical centers conduct?ing research on treatment, prevention, diagnosis, epidemiology, and natural history of HIV infection and disease in pediatric, adolescent, and maternal patient populations, including both domestic and international clinical sites. The NICHD is announcing a competitive Request for Proposal for a Contractor to serve as the NICHD International and Domestic Pediatric and maternal HIV Clinical Studies Coordinating Center, which encompasses both clinical trials on the treatment and management of HIV infection in infants, children, adolescents, and pregnant and non-pregnant women domestically and internationally, including infrastructure development as well as clinical trials. The Coordinating Center contract currently encompasses several inter-related projects: the NICHD Network of clinical trials sites; the Latin American/Caribbean NICHD International Site Development Initiative (NISDI); a trial of post-exposure prophylaxis of HIV-exposed infants (NICHD/HPTN 040 Trial); the India Perinatal Project; and site monitoring for phase III investigator-initiated clinical trials. The current contractor for this effort is Westat, Inc. Scope of activities: Current activities conducted within the Coordinating Center contract include the following: NICHD International and Domestic Pediatric and Maternal HIV Clinical Trials Network The NICHD International and Domestic Pediatric and Maternal HIV Clinical Trials Network (NICHD Network) has been funded through the NICHD Coordinating Center contract since 1987. The NICHD Network consists of domestic and international clinical sites that enroll study subjects in trials related to preventing and treating HIV infection and its complications in neonates, infants, children, adolescents, and pregnant women, as well as selected clinical trials of gender-specific manifestations of HIV infection in non-pregnant women. The Network enrolls into trials conducted by the Pediatric AIDS Clinical Trials Group (PACTG) and Adult ACTG funded by the National Institute of Allergy and Infectious Diseases (NIAID), the NICHD-funded Adolescent HIV Medicine Trials Network (ATN), and Pediatric European Network for Treatment of AIDS (PENTA). Domestically, the Network consists of 20 centers, located in 18 cities, in 10 states/territories (including Puerto Rico); there are six international clinical trials sites: five sites in different areas of Brazil, and one in the Bahamas. NICHD also supports laboratory-based pathogenesis-oriented research in the context of clinical trials. The Coordinating Center provides support to clinical trials site investigators with special laboratory expertise for the conduct of specialized pathogenesis-based studies in the context of PACTG protocols. The Coordinating Center provides special support to international sites, such as providing specimen transport through a central Coordinating Center contract with World Courier. Latin American/Caribbean NICHD International Site Development Initiative Through the experience of the NICHD Network with directly opening antiretroviral drug treatment trials in sites in Brazil and Bahamas in 1998 and 1999, NICHD identified a need for further training and development to increase Latin American and Caribbean capacity for the conduct of clinical trials, particularly those involving experimental drugs. During 2000, NICHD and Coordinating Center began the NICHD International Site Development Initiative in Latin America and the Caribbean (NISDI) to address this need. NISDI is designed to provide capacity-building and training to international sites through the conduct of two observational studies: one in HIV-infected pregnant women and their infants; and the other in HIV-exposed, but uninfected infants and HIV-infected infants, children, and adolescents. The goal of this initiative is to train investigators and develop sites that will be able to participate in future international prevention and treatment trials. The Coordinating Center currently subcontracts with 25 sites in six countries participating in the protocols from Mexico, Argentina, Brazil, Bahamas, Jamaica and Peru. As of July 2006 there were 1,136 pregnant women and 1,522 pediatric patients enrolled into their respective protocols. Clinical Trial of Post-Exposure Prophylaxis of HIV-Exposed Infants in Latin America and the U.S. NICHD, through the Coordinating Center contract, is conducting a study to evaluate the efficacy of antiretroviral prophylaxis provided only to the infant in situations in which the mother has not received any antiretroviral therapy prior to delivery. This includes women who are first identified as HIV-infected during labor, and therefore are unable to receive antepartum or intrapartum prophylaxis. This study compares three different types of post-exposure prophylaxis in such infants standard zidovudine for six weeks to the infant (standard in Brazil and U.S.); a combination of zidovudine with nevirapine; and a triple combination of zidovudine, nevirapine and nelfinavir. The Coordinating Center is responsible for all aspects of clinical trials management, including protocol and forms design, drug repository and dispensation, regulatory issues, data management and data analysis. Participating sites include 6 sites in the US, 8 sites in Brazil, 1 site in Argentina, and 1 site in South Africa in Johannesburg with a second site in Cape Town about to open. India Perinatal Initiative Collaboration with investigators in southern India on a perinatal HIV prevention project was initiated in late 2000, entitled "An observational study of the seroprevalence of, and interventions to decrease the risk of maternal to child transmission of HIV in Tamil Nadu, India". During Stage I of the study, all pregnant women registered in the antenatal clinics were offered the opportunity to participate in an educational session about HIV infection and transmission. Pre- and post-session assessments of knowledge, attitudes, and beliefs were administered to a random sample of women. Voluntary counseling and HIV testing were offered to all women, and the seroprevalence rated was estimated. Enrollment into this part of the protocol took place between December 2003 and December 2004. During Stage II, those women identified as HIV-infected were offered enrollment in a prospective cohort study and offered antiretroviral prophylaxis to prevent mother to child transmission (initially zidovudine, then zidovudine plus single-dose nevirapine). Enrollment into this part of the protocol began in early 2004, and the final subject study visits were completed in May 2006. It is anticipated that close-out of sites, analyses and laboratory testing of stored samples from this study will continue into the new Coordinating Center project period. Site Monitoring of Phase III NICHD-Funded Investigator Initiated International trials As the NICHD international research grant portfolio has increased to include large phase III clinical trials conducted in resource-limited countries, there is an increasing need to ensure that such investigator-initiated trials are conducted ethically, in accordance with Good Clinical Practices, and with attention to human subject safety. The Coordinating Center will conduct site monitoring for selected NICHD grantees conducting large clinical trials to ensure appropriate trial conduct. The Coordinating Center is currently performing site monitoring for the NICHD-funded NEVEREST (Nevirapine Resistance Study) trial evaluating response to therapy in women and children exposed to single-dose nevirapine for prevention of mother to child transmission being conducted in South Africa. It is anticipated that one cost-reimbursement, completion type contract will be awarded, for a period of performance of 5 years, beginning approximately November 1, 2007. RFP-NIH-NICHD CRMC-2008-01 will be available electronically on or about January 29, 2007, with a closing date tentatively set for April 11, 2007 and may be accessed through the FedBizOpps or through the NICHD website at http://www.nichd.nih.gov/funding/grantcontract/, Research and Development Contracts, Contract Opportunities ? Federal Business Opportunities. Offerors are responsible for routinely checking this Web site for any amendments to the solicitation. Any responsible offeror may submit a proposal that will be considered by the Government. This advertisement does not commit the Government to award a contract. No collect calls will be accepted. SEE NOTE 26 Point of contact is Walter A. Knott, Contracting Officer, phone +1 (555) 000-0000, fax +1 (555) 000-0000, e-mail contact@example.gov.

Similar Contracts

Same NAICS industry code

NAICS: 541715
New
Federal
Bolstering Underutilized Industry by Leveraging Technology Transfer (BUILTT) pilot program
Solicitation # 10292026-LR-27
The Department of Energy, in partnership with the National Nuclear Security Administration, has announced the Bolstering Underutilized Industry by Leveraging Technology Transfer (BUILTT) pilot program. This initiative, conducted by the Nevada National Security Sites, Y-12 National Security Complex, and Kansas City National Security Campus, aims to assist qualified U.S. small and medium-sized businesses in manufacturing low-volume, high-impact technologies developed by DOE/NNSA Labs, Plants, and Sites. These technologies, which include specialized optical imaging, radiation and chemical sensing systems, precision electrical components, and advanced materials, often have limited commercial markets but are critical for government mission requirements. Under the program, selected businesses may receive a Cost Reduction License (CRL) for a nominal fee, granting them the rights to produce specified technologies for sale to the DOE, NNSA, and other government customers at pre-negotiated prices. Eligibility is limited to U.S.-based SMBs, with preference given to those near participating sites or those with SBA 8(a) or HUBZone designations. Interested parties are evaluated based on their technical and manufacturing capabilities, financial capacity, and ability to meet regulatory and security requirements. Responses must be submitted to the Technology Partnerships and Intellectual Property Office by April 1, 2027, and are categorized under NAICS code 541715.
Msts – DOE Contractor

POSTED

about 10 hours ago

DEADLINE

in 5 months
View Details
NAICS: 541715
New
Federal
ARTIFICIAL INTELLIGENCE AND NEXT GENERATION DISTRIBUTED COMMAND AND CONTROL
Solicitation # FA875023S7006
The Department of the Air Force, Air Force Materiel Command, AFRL Rome Research Site, is soliciting research and development for Artificial Intelligence and Next Generation Distributed Command and Control under BAA FA8750-23-S-7006. The primary objective is to transform Joint Force Command and Control capabilities by leveraging AI to enhance battlespace assessment, plan selection, and force monitoring in distributed and contested environments. A significant focus is placed on the Battle Management of AI, which seeks technologies to monitor, adapt, and deploy AI capabilities during mission execution to counter model drift and ensure operational safety. This is an open, two-step BAA effective until August 30, 2028, with total estimated funding of approximately $99 million. Individual awards typically range from $200,000 to $20 million and may be awarded as FAR-based procurement contracts, grants, cooperative agreements, or Other Transactions. Initial submissions are limited to three-page white papers, with formal proposals accepted by invitation only. Evaluation is based on a trade-off process considering overall scientific and technical merit, related experience, solution maturity and openness, and cost realism. Prospective offerors must adhere to strict guidelines, including the Gold Standard Science principles for reproducibility and transparency, and must disclose any potential Organizational Conflicts of Interest. Submissions require a CAGE code, unique entity identifier, and an approved DD Form 2345. The government may provide Government Furnished Software for specific technical areas, and all research must comply with National Industrial Security Program standards for the protection of classified information.
FA8750 Afrl Rik

POSTED

about 10 hours ago

DEADLINE

in almost 2 years
View Details
NAICS: 541715
New
Federal
Air Force Research Laboratory (AFRL) Enterprise Commercial Solutions Opening (CSO)
Solicitation # FA865226SC003
The Air Force Research Laboratory (AFRL) Enterprise Commercial Solutions Opening (CSO), solicitation FA8652-26-S-C003, is an overarching enterprise framework designed to acquire innovative commercial products and services. Issued under the authority of 10 USC 3458 and DFARS Subpart 212.70, the CSO establishes a structure for issuing competitive solicitations known as Spirals. These Spirals target a wide range of Areas of Interest (AOI) across the Air, Space, Cyberspace/Electronic Warfare, and Cross-Domain technology domains, including hypersonics, cybersecurity, quantum technologies, and human-machine teaming. Resulting awards may take the form of fixed-price FAR Part 12 contracts or Other Transactions for Prototype (OTP). Foreign participation is strictly prohibited. The acquisition process typically follows a two-step approach for Spirals. In Step One, offerors submit a Commercial Solutions Brief (CSB) consisting of a PowerPoint briefing and a white paper. Those categorized as Selectable are invited to Step Two to submit a full Commercial Solutions Proposal (CSP), which includes a technical proposal, a Statement of Work, and a price proposal with an editable Excel pricing model. Evaluation is conducted via subject-matter expert peer review, focusing on technical merit, applicability, importance to agency programs, and funding availability. Strict security and compliance requirements are in place, including mandatory security risk reviews for all senior and key personnel to mitigate foreign influence. Offerors must also perform an Organizational Conflict of Interest (OCI) analysis and adhere to DoD item unique identification standards (MIL-STD-130) for delivered hardware costing $5,000 or more. Contract administration, including invoicing and payment, is managed electronically through the Wide Area WorkFlow (WAWF) system.
Air Force Research Laboratory

POSTED

about 10 hours ago

DEADLINE

in over 3 years
View Details
NAICS: 541715
New
Federal
Systems for Phenotypic Evaluation, Clinical Trajectories, Response, and Agency (SPECTRA)
Solicitation # ARPA-H-SOL-26-163
The Systems for Phenotypic Evaluation, Clinical Trajectories, Response, and Agency (SPECTRA) program, issued by the Advanced Research Projects Agency for Health (ARPA-H) under solicitation ARPA-H-SOL-26-163, aims to advance the understanding and treatment of autism by identifying evolving developmental trajectories across the lifespan. The program focuses on the nonlinear interactions between genetic, biological, behavioral, and environmental factors to move toward personalized intervention. The scope of work is divided into four Technical Areas: Multi-Factor Analysis and Trajectory Identification (TA1), Population-Scale Modeling and Data Integration (TA2), Precision Intervention and Trajectory Testing (TA3), and Technologies for Communication, Quality of Life, and Embedded Assessment (TA4). Key deliverables include an operating federated network with at least ten live nodes, open-license data standards, a versioned model registry, and the development of technologies that combine clinical assessment with tools to improve daily function and quality of life. Awards will be made via Other Transaction (OT) instruments to proposers determined to be the most advantageous to the government based on scientific merit, capabilities, price/value analysis, and relevance to the ARPA-H mission. The program utilizes a milestone-based acceptance process with gates at 12, 24, and 48 months. Technical requirements emphasize privacy-preserving linkage, differential privacy, and secure execution. Proposers must be registered in SAM.gov and are required to use specific templates for Solution Summaries, with staggered submission deadlines ranging from October 2026 through January 2027. ARPA-H prioritizes entities that will conduct the funded work within the United States.
Advanced Research Projects Agency For Health (arpa-H)

POSTED

about 10 hours ago

DEADLINE

in about 1 month
View Details
NAICS: 541715
New
Grant
2026년도 국제공동연구 신속지원사업 신규과제 공모
Solicitation # 2026-1045
The 2026 International Joint Research Rapid Support Project, solicitation number 2026-1045, is a government-funded initiative managed by the National Research Foundation of Korea and the Ministry of Science and ICT. The project focuses on developing core original technologies for high-density parallel light sources, specifically micro-LED and micro-OLED, for use in AI data center optical interconnects. The total government support funding is 737.5 million KRW for a 16-month performance period running from December 2026 to March 2028. This project is classified as a National Strategic Technology in the semiconductors and next-generation OLED sectors, aiming to advance from Technology Readiness Level 3 to TRL 5. A mandatory requirement for this solicitation is the establishment of an international joint research network with Japanese research institutions to secure expertise in organic light-emitting materials and patents. Technical objectives include developing 32-channel arrays with specific performance targets: transmission speeds exceeding 1 GHz for micro-LED and 0.2 GHz for micro-OLED, and driving energy levels of 1 pJ/bit and 20 pJ/bit respectively. Final acceptance requires the submission of a functional prototype and verification through accredited certification bodies, official test reports, or witnessed self-evaluations. All research achievements and commercialization results must be managed through the Integrated Research Information System (IRIS), and the project is subject to technology fee collection and the 3-book 5-public rule for concurrent research limits.
National Research Foundation of Korea

POSTED

about 13 hours ago

DEADLINE

in 12 days
View Details

Earlier notices in this NAICS code

Posted before this notice, open and closed

Ready to Pursue This Opportunity?

Get AI-powered intelligence on this solicitation and the ones like it

Every page of the solicitation package shredded into a compliance breakdown

AI-powered matching based on your capabilities and past performance

Competitor and incumbent history on the requirement

Automated alerts on amendments, Q&A deadlines, and award

Miguel
Hillary
Keith Deutsch
Christine

Join 750+ contractors already using CLEATUS