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Celebrating 22 YEARS of Regulatory Excellence!
Go with the Most-Trusted Regulations & Guidelines Books on the Market.


Now Available! Revised APRIL 1, 2024 Books!      Also check out our NEW Book:  Good Clinical Practice Regulations in the US & the EU  (Book 1C)!

Book 22:  2024 Frequently Asked Questions and Guidance on Clinical Research from the OHRP

Book 22: 2024 Frequently Asked Questions and Guidance on Clinical Research from the OHRP

$ 17.95

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This spiral-bound, 5" x 7.5" book is a collection of recently finalized guidance documents issued by the US Office for Human Subject Protections (OHRP) under the Department of Health and Human Services.  It includes nearly 100 Frequently Asked Questions on research, as well as brand new guidances on adverse events and research involving children as subjects.

Who Uses this Book?
Investigators, IRB staff, sponsor staff, and anyone else involved in the conduct of biomedical and behavioral research involving human subjects.

What's the Price?
• 1-249 copies:  $17.95             • 250-499 copies:  $16.95
• 500-749 copies: $15.95          • 750+ copies:  $14.95

Custom Cover Prices*?
• 1-24 copies:  unavailable             • 25-100 copies:  $2.00/book
• 100-249 copies: $1.00/book        • 250+ copies:  No charge

* Based on quantities of a single book title

Code of Federal Regulations, 45 CFR Part 46, Protection
   of Human Subjects (As of April 1, 2024)

 • OHRP Frequently Asked Questions on:
        • Assurance Process
        • IRB Registration Process
        Protection of Human Subjects
        • Research with Children
        • Investigator Responsibilities
        • Prisoner Research

 • Reviewing and Reporting Unanticipated Problems
    Involving Risks to Subjects or Others and Adverse
    Events

 • Continuing Review

 • Reporting Incidents to OHRP

 • Written IRB Procedures

 • Guidance on Children Involved as Subjects
    in Research

Click here to see an enlarged pdf cover