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Reagan-Udall Foundation

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uuid000h9kv

Namestring
Reagan-Udall Foundation
Legal namestring
Reagan-Udall Foundation for the FDA
Websiteurl
reaganudall.org
Company typeenum
Private
Founded yearint
2007
Descriptiontext

The Reagan-Udall Foundation for the FDA is an independent 501(c)(3) non-profit organization created by Congress in 2007 to advance the U.S. Food and Drug Administration's regulatory science mission. Headquartered in Washington, D.C., with 11-50 employees, the Foundation operates as a neutral convener and research intermediary between the FDA, regulated industries, academic researchers, healthcare providers, and patient communities. Its work focuses on modernizing product development, accelerating medical innovation, and enhancing safety across drugs, biologics, food, and veterinary products.

The Foundation's portfolio is organized around discrete program areas rather than a unified commercial product. Core tools include the Expanded Access eRequest application and Navigator, which walk physicians and patients step-by-step through the expanded access process for investigational treatments, and the COVID-19 Hub, a centralized public-information resource launched in 2020 in collaboration with FDA's Center for Biologics Evaluation and Research. Research infrastructure centers on IMEDS (Innovation in Medical Evidence Development and Surveillance), providing real-world evidence across more than 110 million people, the Regulatory Science Accelerator for computational modeling and simulation of FDA-regulated products, and targeted programs on substance use disorders (RAISE), rare disease innovation, oncology multi-regional clinical trials, and post-market research. The Foundation also convenes recurring industry roundtables on food traceability, healthy labeling, nutrition incentives, and drug repurposing, and runs the Fellowship in Regulatory Science Innovation to train the next generation of regulatory professionals.

The Foundation does not charge for its public resources, publications, or most services. Revenue is not publicly disclosed, but its operations are sustained by a mix of congressionally authorized status, industry co-funding of specific convenings (e.g., nutrition roundtables funded by Ahold Delhaize USA and H-E-B), and grants supporting individual research programs. Customer-facing activity spans FDA program centers, biopharmaceutical companies, food industry stakeholders, healthcare providers, and patient advocacy organizations, with the FDA acting as both the primary strategic partner and the principal mandate-setter.

Short descriptiontext

The Reagan-Udall Foundation is a Congressionally chartered 501(c)(3) non-profit that serves as an independent convener and research partner for the FDA, advancing regulatory science across drugs, food, and veterinary products. It connects FDA, industry, academia, providers, and patients through tools, research programs, and stakeholder roundtables.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersWashington, United States
HQ citystring
Washington
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
regulatory science research, FDA stakeholder convening, expanded access navigation, real-world evidence research, food safety policy
Industry2 codes
1Regulatory Affairs, Labeling & Advertising/Promotion Compliance
CodeHLAJADAIPrimaryYes
2Clinical Trials Authorization & Oversight (GCP)
CodeHLAJADAFPrimaryNo
NAICS code1 code
  • Scientific Research and Development Services5417
SIC code1 code
  • Services-Commercial Physical & Biological Research8731
Product category
Regulatory Science Research
Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels2 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Personnel, Operations, Others, Marketing or Sales, Technology or R&D
GTM typeB2B
B2B
Offering typeServices
Services
Brand1 of 8 records shown
1Expanded Access eRequest
Description

An online tool that walks physicians and healthcare providers step-by-step through the expanded access process.

reaganudall.org
+7 more records
Core offering1 text field

The Reagan-Udall Foundation for the FDA is an independent 501(c)(3) non-profit created by Congress to advance regulatory science and support the FDA's mission of modernizing product development, accelerating innovation, and enhancing product safety. It delivers a portfolio of public-facing tools (Expanded Access eRequest app and Navigator), research programs (IMEDS real-world evidence, Regulatory Science Accelerator, Real World Data, RAISE), stakeholder convenings (rare disease, oncology clinical trials, food traceability, healthy claim roundtables), and educational resources on FDA-regulated products for healthcare providers, patients, industry, and FDA itself.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 value
  • IMEDS research portfolio covers healthcare experience of more than 110 million people
Product overview1 text field

The Reagan-Udall Foundation is a non-profit foundation that serves as a convening organization to advance the FDA's mission of modernizing product development, accelerating innovation, and enhancing product safety. Rather than offering a unified commercial software product, the Foundation provides a portfolio of public-facing tools, research programs, and stakeholder convening initiatives. Key products include the Expanded Access eRequest app and Navigator, which help physicians and patients navigate the expanded access process; the COVID-19 Hub providing centralized COVID-19 information; and the IMEDS research program delivering real-world evidence on healthcare. The Foundation operates through multiple program areas including Food & Nutrition, Regulatory Science, Substance Use Disorders, and Rare Disease Innovation, offering publications, roundtables, educational resources, and engagement platforms rather than traditional commercial products.

Product and service12 records
1Expanded Access eRequest
CategoryExpanded Access Navigation Tool
Description

Online application that walks physicians and healthcare providers step-by-step through the expanded access process for obtaining investigational treatments for patients.

2Expanded Access Navigator
CategoryExpanded Access Navigation Resource
Description

Comprehensive resource and tool helping patients, providers, and consumers navigate the expanded access process for investigational treatments.

3COVID-19 Hub
CategoryPublic Health Information Resource
Description

Centralized resource providing science-based information on COVID-19 regarding medical response, food and veterinary safety, clinical trials, and vaccine confidence.

4IMEDS (Innovation in Medical Evidence Development and Surveillance)
CategoryReal-World Evidence Research Program
Description

Research program providing real-world insight into the healthcare experience of more than 110 million people, focusing on medical evidence development and post-market surveillance.

5Regulatory Science Accelerator
CategoryRegulatory Science Research Initiative
Description

Computational modeling and simulation initiative supporting innovation in regulatory science for FDA-regulated products.

6Food & Nutrition Programs
CategoryFood and Nutrition Regulatory Program
Description

Multiple initiatives supporting FDA's Nutrition Innovation Strategy, including food traceability, healthy claim roundtables, nutrition communications, and produce safety dialogue.

7Substance Use Disorders Research (RAISE Program)
CategoryPublic Health Research Program
Description

Research and analysis programs addressing substance use disorders, supporting evidence-based approaches to addiction and treatment.

8Real World Data Program
CategoryReal-World Evidence Research
Description

Research initiatives leveraging real-world data to assess the long-term impact of FDA food-related regulations and policies.

9Rare Disease Innovation Roundtable
CategoryStakeholder Convening Initiative
Description

Stakeholder roundtable focused on advancing innovation for rare disease treatments and regulatory approaches.

10Oncology Multi-Regional Clinical Trials Initiative
CategoryClinical Trials Convening Initiative
Description

Initiative to improve the design and conduct of oncology clinical trials across multiple regions.

11COVID-19 Vaccine Confidence Project
CategoryPublic Health Education Project
Description

Project providing information to address COVID-19 vaccine hesitancy by explaining the vaccine development process, safety, and FDA's role in review and authorization.

12Fellowship in Regulatory Science Innovation
CategoryEducation and Training Program
Description

Fellowship program designed to train the next generation of regulatory science professionals.

Scale indicator1 record

Each record includes

Type, Value, Description, Source

Partnership3 partners
Strategic tierCoreTypeStrategic or Co-development Partner
Description

Primary partner in advancing FDA's regulatory science mission. Collaborates on initiatives including drug repurposing frameworks, food safety rules, nutrition policy, and COVID-19 response. The Foundation convenes meetings and develops recommendations in collaboration with FDA programs including the Center for Biologics Evaluation and Research.

Strategic tierMinorTypeGTM or Marketing Partner
Description

Selected to provide public comment at an FDA public meeting on drug repurposing criteria and prioritization, demonstrating the Foundation's role in facilitating industry engagement with FDA regulatory processes.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Collaborated with the Foundation on the COVID-19 Vaccine Confidence Project to better understand perceptions leading to vaccine hesitancy and identify credible messages and messengers.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeRegional player
Description

Industry trade association that engages with FDA on regulatory policy and represents biopharmaceutical companies. Adjacent to the Foundation's industry-convening role but represents commercial members rather than serving as neutral convener.

TypeBroad incumbent
Description

Global professional association for regulatory science and drug development, convening industry, regulators, and academia. Comparable neutral-convener role across the regulatory ecosystem.

TypeDirect peer
Description

Independent non-profit that collaborates with FDA on regulatory science, drug development tools, and data-driven methodologies. Highly comparable in mission, structure, and FDA-relationship model.

TypeBroad incumbent
Description

Congressionally-chartered institution that produces consensus reports on FDA-regulated topics including drug safety, nutrition, and food policy. Comparable federally-sanctioned research and convening authority.

TypeDirect peer
Description

Non-profit focused on accelerating medical research and patient access to treatments through stakeholder engagement and policy work. Operates similar convening and patient access functions.

TypeEmerging player
Description

Non-profit patient advocacy organization engaging with FDA on expanded access, clinical trials, and patient engagement. Comparable focus on patient access and FDA patient listening initiatives.

TypeDirect peer
Description

Non-profit policy advocacy organization that drives regulatory innovation and partners with FDA on cancer drug development frameworks. Comparable convening role and FDA collaboration model.

TypeBroad incumbent
Description

University-affiliated policy center producing FDA-relevant regulatory science research and convening stakeholders on drug development, real-world evidence, and value-based care. Comparable research-and-convening mandate.

TypeDirect peer
Description

Independent non-profit research organization funded through Congress that funds comparative clinical effectiveness research and convenes stakeholders. Comparable congressional mandate and patient-outcomes focus.

10ClinicalTrials.gov (NIH/NLM)
TypeEmerging player
Description

Government public resource for clinical trial registration and results reporting, addressing patient/provider access to trial information. Comparable public-information infrastructure function for FDA-regulated products.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 records

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Competitive moat4 records

Each record includes

Type, Details

Key risks5 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment4 records

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Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile4 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
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Number of profiles
No data
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Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

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Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Reagan-Udall Foundation

Regulatory Science Researchreaganudall.org

The Reagan-Udall Foundation is a Congressionally chartered 501(c)(3) non-profit that serves as an independent convener and research partner for the FDA, advancing regulatory science across drugs, food, and veterinary products. It connects FDA, industry, academia, providers, and patients through tools, research programs, and stakeholder roundtables.

What Reagan-Udall Foundation does

The Reagan-Udall Foundation for the FDA is an independent 501(c)(3) non-profit organization created by Congress in 2007 to advance the U.S. Food and Drug Administration's regulatory science mission. Headquartered in Washington, D.C., with 11-50 employees, the Foundation operates as a neutral convener and research intermediary between the FDA, regulated industries, academic researchers, healthcare providers, and patient communities. Its work focuses on modernizing product development, accelerating medical innovation, and enhancing safety across drugs, biologics, food, and veterinary products.

The Foundation's portfolio is organized around discrete program areas rather than a unified commercial product. Core tools include the Expanded Access eRequest application and Navigator, which walk physicians and patients step-by-step through the expanded access process for investigational treatments, and the COVID-19 Hub, a centralized public-information resource launched in 2020 in collaboration with FDA's Center for Biologics Evaluation and Research. Research infrastructure centers on IMEDS (Innovation in Medical Evidence Development and Surveillance), providing real-world evidence across more than 110 million people, the Regulatory Science Accelerator for computational modeling and simulation of FDA-regulated products, and targeted programs on substance use disorders (RAISE), rare disease innovation, oncology multi-regional clinical trials, and post-market research. The Foundation also convenes recurring industry roundtables on food traceability, healthy labeling, nutrition incentives, and drug repurposing, and runs the Fellowship in Regulatory Science Innovation to train the next generation of regulatory professionals.

The Foundation does not charge for its public resources, publications, or most services. Revenue is not publicly disclosed, but its operations are sustained by a mix of congressionally authorized status, industry co-funding of specific convenings (e.g., nutrition roundtables funded by Ahold Delhaize USA and H-E-B), and grants supporting individual research programs. Customer-facing activity spans FDA program centers, biopharmaceutical companies, food industry stakeholders, healthcare providers, and patient advocacy organizations, with the FDA acting as both the primary strategic partner and the principal mandate-setter.

Reagan-Udall Foundation firmographics

Firmographics
Name
Reagan-Udall Foundation
Legal name
Reagan-Udall Foundation for the FDA
Website
https://reaganudall.org
Company type
Private
Founded year
2007
Operating status
Operating
Headcount range
11–50 employees
Short description
The Reagan-Udall Foundation is a Congressionally chartered 501(c)(3) non-profit that serves as an independent convener and research partner for the FDA, advancing regulatory science across drugs, food, and veterinary products. It connects FDA, industry, academia, providers, and patients through tools, research programs, and stakeholder roundtables.
Ownership category
akta.pro rank

Reagan-Udall Foundation industry classification

Industry
Product category
Regulatory Science Research
NAICS
Scientific Research and Development Services (5417)
SIC
Services-Commercial Physical & Biological Research (8731)
akta.pro primary industry
Regulatory Affairs, Labeling & Advertising/Promotion Compliance (HLAJADAI)
akta.pro secondary industry
Clinical Trials Authorization & Oversight (GCP) (HLAJADAF)

Keywords

  • Regulatory science research
  • FDA stakeholder convening
  • Expanded access navigation
  • Real-world evidence research
  • Food safety policy

Where Reagan-Udall Foundation is headquartered

Location

Headquarters

HQ city
Washington
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Reagan-Udall Foundation business model

Business model
GTM type
B2B
Offering type
Services
Cost components
Personnel, Operations, Others, Marketing or Sales, Technology or R&D

Distribution channels2 records

Marketing channels4 records

Reagan-Udall Foundation product offering

Product offering

Core offering

The Reagan-Udall Foundation for the FDA is an independent 501(c)(3) non-profit created by Congress to advance regulatory science and support the FDA's mission of modernizing product development, accelerating innovation, and enhancing product safety. It delivers a portfolio of public-facing tools (Expanded Access eRequest app and Navigator), research programs (IMEDS real-world evidence, Regulatory Science Accelerator, Real World Data, RAISE), stakeholder convenings (rare disease, oncology clinical trials, food traceability, healthy claim roundtables), and educational resources on FDA-regulated products for healthcare providers, patients, industry, and FDA itself.

Product overview

The Reagan-Udall Foundation is a non-profit foundation that serves as a convening organization to advance the FDA's mission of modernizing product development, accelerating innovation, and enhancing product safety. Rather than offering a unified commercial software product, the Foundation provides a portfolio of public-facing tools, research programs, and stakeholder convening initiatives. Key products include the Expanded Access eRequest app and Navigator, which help physicians and patients navigate the expanded access process; the COVID-19 Hub providing centralized COVID-19 information; and the IMEDS research program delivering real-world evidence on healthcare. The Foundation operates through multiple program areas including Food & Nutrition, Regulatory Science, Substance Use Disorders, and Rare Disease Innovation, offering publications, roundtables, educational resources, and engagement platforms rather than traditional commercial products.

Differentiator

Problem solved

Functional benefit

Brands

  • Expanded Access eRequest: An online tool that walks physicians and healthcare providers step-by-step through the expanded access process.
  • Navigator
  • COVID-19 Hub
  • COVID-19 Vaccine Confidence Project
  • IMEDS
  • Real World Data
  • RAISE
  • Regulatory Science Accelerator

Products and services

  • Expanded Access eRequest Online application that walks physicians and healthcare providers step-by-step through the expanded access process for obtaining investigational treatments for patients.
  • Expanded Access Navigator Comprehensive resource and tool helping patients, providers, and consumers navigate the expanded access process for investigational treatments.
  • COVID-19 Hub Centralized resource providing science-based information on COVID-19 regarding medical response, food and veterinary safety, clinical trials, and vaccine confidence.
  • IMEDS (Innovation in Medical Evidence Development and Surveillance) Research program providing real-world insight into the healthcare experience of more than 110 million people, focusing on medical evidence development and post-market surveillance.
  • Regulatory Science Accelerator Computational modeling and simulation initiative supporting innovation in regulatory science for FDA-regulated products.
  • Food & Nutrition Programs Multiple initiatives supporting FDA's Nutrition Innovation Strategy, including food traceability, healthy claim roundtables, nutrition communications, and produce safety dialogue.
  • Substance Use Disorders Research (RAISE Program) Research and analysis programs addressing substance use disorders, supporting evidence-based approaches to addiction and treatment.
  • Real World Data Program Research initiatives leveraging real-world data to assess the long-term impact of FDA food-related regulations and policies.
  • Rare Disease Innovation Roundtable Stakeholder roundtable focused on advancing innovation for rare disease treatments and regulatory approaches.
  • Oncology Multi-Regional Clinical Trials Initiative Initiative to improve the design and conduct of oncology clinical trials across multiple regions.
  • COVID-19 Vaccine Confidence Project Project providing information to address COVID-19 vaccine hesitancy by explaining the vaccine development process, safety, and FDA's role in review and authorization.
  • Fellowship in Regulatory Science Innovation Fellowship program designed to train the next generation of regulatory science professionals.

Quantifiable outcome

  • IMEDS research portfolio covers healthcare experience of more than 110 million people

Companies that use Reagan-Udall Foundation

Customer profile

Segments4 records

Ideal customer profiles4 records

Reagan-Udall Foundation technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

Reagan-Udall Foundation partnerships and signals

Strategic signal

Partnerships

Three partnerships are on record, tiered core and minor.

  • U.S. Food and Drug Administration (FDA)coreStrategic or Co-development PartnerPrimary partner in advancing FDA's regulatory science mission. Collaborates on initiatives including drug repurposing frameworks, food safety rules, nutrition policy, and COVID-19 response. The Foundation convenes meetings and develops recommendations in collaboration with FDA programs including the Center for Biologics Evaluation and Research.
  • Palvella TherapeuticsminorGTM or Marketing PartnerSelected to provide public comment at an FDA public meeting on drug repurposing criteria and prioritization, demonstrating the Foundation's role in facilitating industry engagement with FDA regulatory processes.
  • FDA Center for Biologics Evaluation and ResearchcoreStrategic or Co-development PartnerCollaborated with the Foundation on the COVID-19 Vaccine Confidence Project to better understand perceptions leading to vaccine hesitancy and identify credible messages and messengers.

Scale indicators1 record

Recent moves6 records

Expansion highlights5 records

Reagan-Udall Foundation competitors and assessment

Company assessment

Regional players

  • Biotechnology Innovation Organization (BIO): Industry trade association that engages with FDA on regulatory policy and represents biopharmaceutical companies. Adjacent to the Foundation's industry-convening role but represents commercial members rather than serving as neutral convener.

Broad incumbents

  • Drug Information Association (DIA): Global professional association for regulatory science and drug development, convening industry, regulators, and academia. Comparable neutral-convener role across the regulatory ecosystem.
  • National Academies of Sciences, Engineering, and Medicine: Congressionally-chartered institution that produces consensus reports on FDA-regulated topics including drug safety, nutrition, and food policy. Comparable federally-sanctioned research and convening authority.
  • Duke-Margolis Center for Health Policy: University-affiliated policy center producing FDA-relevant regulatory science research and convening stakeholders on drug development, real-world evidence, and value-based care. Comparable research-and-convening mandate.

Direct peers

  • Critical Path Institute: Independent non-profit that collaborates with FDA on regulatory science, drug development tools, and data-driven methodologies. Highly comparable in mission, structure, and FDA-relationship model.
  • FasterCures (Milken Institute): Non-profit focused on accelerating medical research and patient access to treatments through stakeholder engagement and policy work. Operates similar convening and patient access functions.
  • Friends of Cancer Research: Non-profit policy advocacy organization that drives regulatory innovation and partners with FDA on cancer drug development frameworks. Comparable convening role and FDA collaboration model.
  • Patient-Centered Outcomes Research Institute (PCORI): Independent non-profit research organization funded through Congress that funds comparative clinical effectiveness research and convenes stakeholders. Comparable congressional mandate and patient-outcomes focus.

Emerging players

  • National Patient Advocate Foundation: Non-profit patient advocacy organization engaging with FDA on expanded access, clinical trials, and patient engagement. Comparable focus on patient access and FDA patient listening initiatives.
  • ClinicalTrials.gov (NIH/NLM): Government public resource for clinical trial registration and results reporting, addressing patient/provider access to trial information. Comparable public-information infrastructure function for FDA-regulated products.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat4 records

Key risks5 records

Key highlights7 records

Customer concentration

Reagan-Udall Foundation social profiles

Digital presence

Reagan-Udall Foundation financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Reagan-Udall Foundation leadership team

Management profile

Number of profiles

Reagan-Udall Foundation funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Reagan-Udall Foundation M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Reagan-Udall Foundation

What does Reagan-Udall Foundation do?

The Reagan-Udall Foundation for the FDA is an independent 501(c)(3) non-profit created by Congress to advance regulatory science and support the FDA's mission of modernizing product development, accelerating innovation, and enhancing product safety. It delivers a portfolio of public-facing tools (Expanded Access eRequest app and Navigator), research programs (IMEDS real-world evidence, Regulatory Science Accelerator, Real World Data, RAISE), stakeholder convenings (rare disease, oncology clinical trials, food traceability, healthy claim roundtables), and educational resources on FDA-regulated products for healthcare providers, patients, industry, and FDA itself.

Is Reagan-Udall Foundation a public or private company?

Reagan-Udall Foundation is a private company. It is classified as nonprofit foundation owned and is currently operating.

When was Reagan-Udall Foundation founded?

Reagan-Udall Foundation was founded in 2007. It employs 11 to 50 people.

Where is Reagan-Udall Foundation based?

Reagan-Udall Foundation is headquartered in Washington, United States, in the North America region.

Who are Reagan-Udall Foundation's main competitors?

Biotechnology Innovation Organization (BIO) is listed as a regional player. Broad incumbents are Drug Information Association (DIA), National Academies of Sciences, Engineering, and Medicine and Duke-Margolis Center for Health Policy. Direct peers are Critical Path Institute, FasterCures (Milken Institute), Friends of Cancer Research and Patient-Centered Outcomes Research Institute (PCORI). Emerging players are National Patient Advocate Foundation and ClinicalTrials.gov (NIH/NLM).

Does Reagan-Udall Foundation have an API?

No public API is recorded for Reagan-Udall Foundation.

What industry is Reagan-Udall Foundation in?

Reagan-Udall Foundation's product category is Regulatory Science Research. Its primary akta.pro industry code is HLAJADAI, Regulatory Affairs, Labeling & Advertising/Promotion Compliance, with a secondary code of HLAJADAF, Clinical Trials Authorization & Oversight (GCP). Its NAICS code is 5417 and its SIC code is 8731.

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Live signals
The National Law ReviewRecommendations Related to Infant Formula Safety Provided by RepoThe Reagan-Udall Foundation released a report on infant formula safety after 2025-2026 recalls linked to Clostridium botulinum. It outlines five key areas, including data sharing and FDA collaboration, and calls for industry-wide collaboration to develop credible, feasible solutions.AhiAHI Supports Reagan-Udall Foundation Report on Modernizing the Center for Veterinary MedicineThe American Horse Council (AHI) endorsed the Reagan-Udall Foundation's report advocating for modernization of the Center for Veterinary Medicine (CVM). The organization supports specific regulatory reforms, such as reducing raw data submission burdens and utilizing mathematical modeling, to accelerate innovation and lower costs in veterinary drug development. AHI intends to collaborate with the CVM and Congress to implement these changes, aiming to enhance animal health products and manufacturing within the United States.National Center for Biotechnology InformationScientific Advancements in Gene Therapies: Opportunities for Global Regulatory ConvergenceThe Reagan-Udall Foundation for the FDA, in collaboration with the FDA and the Gates Foundation, hosted a workshop on September 4, 2024, to discuss strategies for global regulatory convergence and equitable access to gene therapies in low- and middle-income countries. The event highlighted significant barriers such as high costs, regulatory gaps, and infrastructure deficits, while exploring solutions like local manufacturing capacity and harmonized regulatory frameworks. Key discussions focused on addressing ethical concerns, improving public engagement, and leveraging technologies like CRISPR to treat prevalent diseases such as sickle cell disease.FoodreadyHow To Implement the Food Traceability 204 Rule?The article provides a step-by-step guide for food manufacturers to implement the FDA's FSMA Rule 204, which mandates enhanced traceability records with a compliance deadline of January 2026. It outlines key preparation steps such as gap assessments, supply chain mapping, and technology adoption, while highlighting challenges like implementation costs and interoperability issues. The text also references industry collaborations led by organizations like GS1 US and the Reagan-Udall Foundation to address these regulatory hurdles.YouTubeAdvancing Real-World Data to Generate Regulatory Grade Real-World Evidence in OncologyOn February 20, Friends of Cancer Research, Duke-Margolis Institute for Health Policy, Reagan-Udall Foundation for the FDA and Aetion co-hosted a workshop on generating regulatory-grade real-world evidence in oncology. Participants including regulators, clinicians, patients, advocates, data vendors and biopharma representatives discussed gaps in data collection, accessibility, quality and patient care relevance, and the U.S. regulatory framework. The event concluded with an open conversation on remaining challenges and next steps.PR NewswireFDA Provides Update on External Evaluation to Strengthen Agency's Tobacco ProgramFDA Commissioner Robert M. Califf announced on December 19, 2022, that an external expert panel facilitated by the Reagan-Udall Foundation has released its findings and recommendations from an evaluation of the FDA's Tobacco Program. The Center for Tobacco Products leadership will review the report and provide an update on next steps by early February. The evaluation comes amid public health concerns, including nearly 500,000 annual deaths from cigarette smoking and over 3 million youth reporting current tobacco product use in 2022.PR NewswireCOVID-19 Research Database Recognized by the Reagan-Udall Foundation for the FDA for Accelerating Breakthrough ResearchThe Reagan-Udall Foundation for the FDA awarded the COVID-19 Research Database the 2021 Innovations in Regulatory Science Award, recognizing its novel public-private collaboration framework that has enabled over 3,000 researchers to conduct more than 300 studies on the pandemic. PointClickCare also announced that de-identified long-term care data covering billions of patient encounters from over 21,000 skilled nursing facilities, senior living communities, and home health agencies is now accessible to researchers through the database. The initiative, led by multiple healthcare organizations including Change Healthcare, Datavant, Health Care Cost Institute, Healthjump, Medidata, Mirador Analytics, Office Ally, PointClickCare, SAS, StataCorp, Snowflake, and Veradigm, aims to serve as a blueprint for future collaborative research efforts.PR NewswireRDBA and FDA Foundation Partner to Provide Turnkey Resources to Retail DietitiansThe Reagan-Udall Foundation for the FDA (FDA Foundation) and the Retail Dietitians Business Alliance (RDBA) jointly launched the Ultimate Retail Dietitians Toolkit, providing free science-based resources including social media templates, fact sheets, recipes, and educational materials for retail dietitians. The toolkit, built around the FDA's new Nutrition Facts label and the Dietary Guidelines for Americans 2020-2025, aims to support retail dietitians in helping consumers adopt healthier eating habits. The free resources are available to all registered dietitians on the RDBA website.