Skip to content
  • Login to WCG IRB Connexus
WCG IRB logo Toggle Menu
  • Services
      • IRB Review ServicesFor more than 50 years, we’ve set the standard for IRB review through service, expertise, and innovation.
      • IBC Administration & ReviewSince 2000, we’ve provided Institutional Biosafety Committee services to nearly 800 institutions in 14 countries.
      • Our Leading IRB Submission Portal
      • Expanded Access / Compassionate Use
      • Independent Review Services
      • Services For
      • Institutions
      • Investigators
      • Sponsors & CROs
      • Research Participants
  • How to Submit
      • How to Submit for IRB Review
      • Download IRB Forms
      • Request a Fee Schedule
      • How to Submit for IBC Review
      • Download IBC Forms
      • Resources
      • Download Resources
      • Frequently Asked Questions
      • Login to WCG IRB Connexus
  • Insights
    • Ethical Review Insights
    • Biosafety Insights
    • Ask the IRB and IBC Experts
    • Case Studies
    • News & Events
    • COVID-19 Resource Center
    • WCG Institute
    • WCG Podcast
  • About Us
    • About WCG IRB
    • Leadership & Advisory Boards
    • Compliance Statement
    • IRB Registration & FWA
    • News & Events
    • Careers
  • Contact Us

Ethics Insights

Viewing all entries for: ethics

  • Insights
    • Insights Archive
      • ethics
Ask the Experts

Caregivers as Research Participants

Read More about Caregivers as Research Participants
Doctor talking to Nurse about an X-ray Ask the Experts

Employees as Research Participants

Read More about Employees as Research Participants
business people talking at table Videos

Understanding the FDA’s new proposed regulations on human subject research and their impact on your clinical trial plans

Read More about Understanding the FDA’s new proposed regulations on human subject research and their impact on your clinical trial plans
Blog Posts

Assessing Potential Risks in the Consideration of IND Exemption Criteria

Read More about Assessing Potential Risks in the Consideration of IND Exemption Criteria
Blog Posts

Defining “Minimal Risk” in Clinical Research

Read More about Defining “Minimal Risk” in Clinical Research
Doctor with mom and child Ask the Experts

Should Parents Be Allowed to View their Child’s Survey Responses?

Read More about Should Parents Be Allowed to View their Child’s Survey Responses?
Whitepapers

Drafting a Research Plan for IRB Review and Research Conduct: Information that Must Be Included in a Clinical Trial Protocol

Read More about Drafting a Research Plan for IRB Review and Research Conduct: Information that Must Be Included in a Clinical Trial Protocol
Women collaborating in an office, looking at charts on a tablet. Whitepapers

Do You Know Me?: The Subtle Distinction Between “Anonymous” and “De-identified” Data in Clinical Research

Read More about Do You Know Me?: The Subtle Distinction Between “Anonymous” and “De-identified” Data in Clinical Research
Person using tablet to review medical records. Ask the Experts

Does research involving retrospective review of patient charts require IRB review?

Read More about Does research involving retrospective review of patient charts require IRB review?
Toolbox Medical Innovations Logo Case Studies

Toolbox Medical Relies on WCG IRB’s Prompt, Personalized Expertise in an Unsettled Environment

Read More about Toolbox Medical Relies on WCG IRB’s Prompt, Personalized Expertise in an Unsettled Environment
  • Content Type
    • Ask the Experts
    • Blog Posts
    • Case Studies
    • News & Events
    • Videos
    • Whitepapers

Tags

  • adverse events
  • advertising
  • assent form
  • biosafety
  • case study
  • centralized review
  • challenge studies
  • child subjects
  • COI
  • common rule
  • compensation
  • Connexus
  • consent
  • coverage analysis
  • covid-19
  • data
  • decentralized
  • deviations
  • Diversity
  • e-consent
  • eligibility
  • ethics
  • expanded access
  • FDA Review
  • gene therapy
  • gene transfer
  • hipaa
  • human factors
  • incentives
  • infectious disease
  • informed consent
  • Institutional Biosafety Committee
  • investigational
  • IRB Review
  • LGBTQIA+
  • medical devices
  • observational studies
  • oncology
  • patient screening
  • payments
  • pragmatic clinical trials
  • privacy
  • protocol deviations
  • recruitment
  • reimbursement
  • remote assessment
  • reporting
  • staffing
  • stem cells
  • training
  • translations
  • vaccine
  • virtual trials
Viewing 1 - 10 of 21 articles
  • 1
  • 2
  • 3
  • Next
  • WCG Privacy Policy
  • WCG Terms of Use
  • Sitemap
  • Do Not Sell Or Share My Data

Copyright 2023 WCG IRB. All rights reserved.