Release date: February 2017
Valid through: February 2020
This activity is intended for clinical trial research physicians and nurses.
- The 21st Century Cures Act easily passed, but is it good for research protection?
- Vulnerable people are a cornerstone of human research protections
- A list of vulnerable populations exploited in U.S. research
- IRB’s new member handbook improves IRB training
- VCU IRB’s member handbook covers what they need to know
- Reimagining the IRB model for the 21st century
- The ethical question of denying children antibiotics
- ‘Serious noncompliance’ the leading issue reported to OHRP
- 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.
- Maximum of 1.5 AMA PRA Category 1 Credits™
This activity is sponsored by AHC Media.
AHC Media is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.
AHC Media designates this enduring material for a maximum of 1.5 AMA PRA Category 1 Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
Melinda Young, Gary Evans
Physician Editor: Lindsay McNair, MD, MPH, MSB
Nurse Planner: Kay Ball, RN, PhD
AHC Media Editor: Jill Drachenberg
Ebook Design Specialist: Dana Spector
Contributing Editor Melinda Young, Medical Writer Gary Evans, Editor Jill Drachenberg, Ebook Design Specialist Dana Spector, Physician Editor Lindsay McNair, MD, MPH, MSB, and Nurse Planner Kay Ball, RN, PhD, report no consultant, stockholder, speaker’s bureau, research, or other financial relationships with companies having ties to this field of study.
Copyright 2017, AHC Media. All rights reserved.
This course is no longer available to take.