Skip to content
  • Careers
  • Legacy MyConnexus
  • 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.
      • Leading Technology Supporting Ethical Review
      • Expanded Access / Compassionate Use
      • 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
      • Login to Legacy Connexus
  • Insights
    • Ethical Review 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
    • International Fellows Program
    • Compliance Statement
    • IRB Registration & FWA
    • News & Events
    • Careers
  • Contact Us

Insights Archive

View all entries for: adverse events

  • Insights
    • Insights Archive
      • adverse events
Business woman reviewing document Ask the Experts

What are IRB submission requirements for post marketing safety reports?

Read More about What are IRB submission requirements for post marketing safety reports?
stethoscope on medical document and doctor studying data Ask the Experts

Submitting Deviations from a Sponsor’s Adverse Event Reporting Requirements to the IRB

Read More about Submitting Deviations from a Sponsor’s Adverse Event Reporting Requirements to the IRB
man looking at laptop Ask the Experts

What are the IRB Reporting Requirements for Adverse Events?

Read More about What are the IRB Reporting Requirements for Adverse Events?
doctor holding tablet Ask the Experts

Do we need to submit safety events from another site to our IRB?

Read More about Do we need to submit safety events from another site to our IRB?
  • Content Type
    • Ask the Experts
    • Blog Posts
    • Case Studies
    • News & Events
    • Videos
    • Whitepapers

Tags

  • adverse events
  • assent form
  • biosafety
  • centralized review
  • challenge studies
  • child subjects
  • COI
  • common rule
  • compensation
  • consent
  • coverage analysis
  • covid-19
  • data
  • deviations
  • e-consent
  • eligibility
  • ethics
  • expanded access
  • gene therapy
  • gene transfer
  • hipaa
  • IBC
  • incentives
  • infectious disease
  • informed consent
  • investigational
  • medical devices
  • observational studies
  • oncology
  • payments
  • pragmatic clinical trials
  • privacy
  • protocol deviations
  • recruitment
  • reimbursement
  • remote assessment
  • reporting
  • stem cells
  • training
  • translations
  • vaccine
  • virtual trials
Viewing 1 - 4 of 4 articles
  • WCG Privacy Policy
  • WCG Terms of Use
  • Sitemap
  • Do Not Sell My Information

Copyright 2021 WCG IRB. All rights reserved.