Release date: March 2017
Valid through: March 2020
This activity is intended for clinical trial research physicians and nurses.
- Common Rule change took six years to complete — and could be upended in 30 seconds
- Final Common Rule is an improvement, but leaves some questions unanswered
- Best Practices Spotlight: Strategies to better manage noncompliance
- The complicated quest to replicate research
- Clinical trials: More is not necessarily better
- Military IRBs may err on the side of more bureaucracy
- Teleconsent boosts recruitment of rural research subjects
- 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.
Relias Learning, LLC is accredited as a provider of continuing nursing education by the American Nurses Credentialing Center’s Commission on Accreditation.
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
Editor: Dana Spector
Author Melinda Young, Medical Writer Gary Evans, Editor Jill Drachenberg, Editor 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.