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IRB Advisor (Vol. 19, No. 10) – October 1, 2019

Specialty: Clinical Trial Research Format: Text 
Course #: 14675  Price: $27.00  
Release date: 2019-09-23  Valid through: 2022-10-31  
Publication: This activity appeared in IRB Advisor (CME), published on 2019-10-01. 
Review date: 2019-09-23 
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Learning Objectives

  • Establish clinical trial programs using accepted ethical principles for human subject protection
  • Apply the mandated regulatory safeguards for patient recruitment, follow-up and reporting of findings for human subject research
  • Comply with the necessary educational requirements regarding informed consent and human subject research

Accreditation Statement

Relias LLC is accredited by the Accreditation Council for Continuing Medical Education (ACCME) to provide continuing medical education for physicians.

Credit Designation

Relias LLC designates this enduring material for a maximum of 1.5 AMA PRA Category 1 Credits™. Physicians should claim only credit commensurate with the extent of their participation in the activity.

Financial Disclosure

Author Melinda Young, Medical Writer Gary Evans, Editor Jill Drachenberg, Editor Jonathan Springston, Editorial
Group Manager Leslie Coplin, and Physician Editor Lindsay McNair, MD, MPH, MSBioethics, report no consultant, stockholder, speaker’s
bureau, research, or other financial relationships with companies having ties to this field of study. Nurse Planner Kay Ball, PhD, RN, CNOR,
CMLSO, FAAN, is a consultant for Ethicon USA and Mobile Instrument Service and Repair.

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