Sitemap - 2026 - Science Policy Insights in Research & Technology (SPIRIT)

The Science Policy Scoop (Week of July 20, 2026)

Human Research Standards Organization (HRSO) and Human Research Accreditation Canada (HRA Canada)

ClinicalTrials.gov Gets a Research Partner

FDA and EU/EMA Common Technical Document (CTD) Requirements

The Science Policy Scoop (Week of July 13, 2026)

Addressing Consent-based Challenges to Improve Inclusivity in Research

What Walking Backwards Taught Me About Research Ethics and Compliance

The Science Policy Scoop (Week of July 6, 2026)

The Word They Almost Used: Bioethics' Unfinished Argument Over Patient, Subject, and Participant

The Federal and Congressional Scoop on Research (June 2026)

The Gold Standard for Science: Does OMB’s Grant Reform Measure Up?

The Science Policy Scoop (Week of June 15, 2026)

Why Applied Research Ethics Matters in Human Subjects Research

The Science Policy Scoop (Week of June 8, 2026)

Accelerating the Scientific Enterprise: What Did the Research Community Tell OSTP and Will OMB Listen?

The Science Policy Scoop (Week of June 1, 2026)

The Federal and Congressional Scoop on Research (May 2026)

Chat- IRB? How Application-specific Language Models can Enhance Research Ethics Review

ClinicalTrials.gov 101 for Study Teams and IRBs

What If Federal Research Compliance Moved Under One New Assistant Secretary?

The Science Policy Scoop (Week of May 18, 2026)

Ethical Violations in Clinical Research: Comparing Two FDA Warning Letters Through the Belmont Report

The Science Policy Scoop (Week of May 11, 2026)

The Science Policy Scoop (Week of May 4, 2026)

Inside Advocacy Behind the Responsible Conduct of Research (RCR) (May 2026)

The Federal and Congressional Scoop on Research (April 2026)

The Science Policy Scoop (Week of April 20, 2026)

The Science Policy Scoop (Week of April 13, 2026)

The Science Policy Scoop (Week of April 6, 2026)

How Do I Know What You're Using My Survey Responses for?

The Federal and Congressional Scoop on Research (March 2026)

Former FDA BIMO Investigator: What IRBs Can Do to Stay Compliant

The Med Writer’s Notebook

Inside the FDA, HHS, and the NIH

Inside Advocacy Behind the Responsible Conduct of Research (RCR)

Introducing the RAC Podcast Summarizer

Former OHRP Klote on Navigating the Evolving Federal Landscape in Research

Inside the FDA, HHS, and the NIH