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Copernicus Group – Independent Review Board

Experience and innovation in ethical review®

 
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    "I like knowing you are there to help me do my job."
    — Research Director

    Home > Investigators > Research Responsibilities
 

Research Responsibilities

Click on the following links to review US FDA guidelines and responsibilities:

  • Good Clinical Practice (US FDA)
  • FDA Information Sheets (US FDA)
  • Informed Consent Process (US FDA)
  • HIPAA Privacy Rule Information for Researchers (US DHHS)
  • Subject Recruitment (US FDA)
  • Awareness of state and local research laws (US FDA)

 

 
  • About
    • Mission, Vision & Values
    • Leadership Team
    • Careers
    • Culture
    • Quality Policy
    • Contact Us
    • Feedback
    • Location and Directions
  • IRB Services
    • IRB Services Overview
    • Submission Information
    • Fee Schedule Request
    • Board Review & Actions
    • Translation Services
    • Compliance Statement
    • Meeting Schedule
    • Request IRB Roster
  • Subjects
    • Information For Subjects
    • Deciding to Participate
    • Subjects Rights
    • Who Protects Subjects
    • Resources
    • Request Information
    • FAQs
  • Investigators
    • Services Overview
    • Research Responsibilities
    • Ethical Research Principles
    • Forms
    • Regulatory Guidance
    • GCP Training
    • FAQs
  • Sponsors/CRO
    • Information for Sponsors and CROs
    • Submit a study
    • Forms
    • Resources
    • GCP Training
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  • Institutions
    • Information for Institutions
    • Submit a study
    • Forms
    • Regulatory Guidance
    • GCP Training
    • FAQs
 

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