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University of Arkansas for Medical Sciences

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    • About
      • Compliance Statement
      • Full Board Meetings
        • Current Committee Rosters
        • Previous Committee Rosters
      • Human Research Protection Program Plan
      • IRB Blogs
      • IRB Staff
      • Review Fees
    • CLARA
      • Access the System
      • Start a Study
      • Request a HSR Determination
    • Templates, Training, Tools
      • Consent for Non-English Speakers
      • CITI Training Instructions
    • Reporting
    • Policies
      • Current IRB Policies
      • IRB Policy Archives
    • Research Resources
      • Abbreviations and Acronyms
      • Emergency Use
      • FAQs
      • Reporting to the IRB
      • Single/Central IRB Review
  • Home
  • Institutional Review Board
  • IRB Policies
  • Current IRB Policies
  • 18 Drugs and Devices

18 Drugs and Devices

  • Home
    • Current IRB Policies
      • 01 Principles and Authority
      • 02 Relationships
      • 03 Committee Membership
      • 04 IRB Operations
      • 05 Records (Retired)
      • 06 Documentation
      • 07 Procedures for Study Review
      • 08 Change in Protocol
      • 09 IRB Decisions
      • 10 Principal Investigator Responsibilities
      • 11 Appeals and Reconsiderations (retired)
      • 12 Quality Assurances
      • 13 Confidentiality
      • 14 Recruitment Practices
      • 15 Consent
      • 16 Risk/Benefit Analysis (moved)
      • 17 Special Populations
      • 18 Drugs and Devices
      • 19 Human Genetics Guidance
      • 20 Questions, Concerns, Suggestions and Complaints

IRB Policy 18.1 Review of Investigational New Drug (IND) Studies

IRB Policy 18.2 Investigational Devices

IRB Policy 18.3 Emergency Use of a Test Article

IRB Policy 18.4 Emergency Use of an Unapproved Medical Device (see archive)

  • Home
    • Current IRB Policies
      • 01 Principles and Authority
      • 02 Relationships
      • 03 Committee Membership
      • 04 IRB Operations
      • 05 Records (Retired)
      • 06 Documentation
      • 07 Procedures for Study Review
      • 08 Change in Protocol
      • 09 IRB Decisions
      • 10 Principal Investigator Responsibilities
      • 11 Appeals and Reconsiderations (retired)
      • 12 Quality Assurances
      • 13 Confidentiality
      • 14 Recruitment Practices
      • 15 Consent
      • 16 Risk/Benefit Analysis (moved)
      • 17 Special Populations
      • 18 Drugs and Devices
      • 19 Human Genetics Guidance
      • 20 Questions, Concerns, Suggestions and Complaints

Contact Us

Institutional Review Board
University of Arkansas for Medical Sciences
4301 W. Markham St.
Slot 636
Little Rock, AR 72205

IRB@uams.edu

501.686.5667 (main line)

Full Accreditation

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IRB has been fully accredited by the Association for the Accreditation of Human Research Protection Programs (AAHRPP) since 2005.

University of Arkansas for Medical Sciences

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