Release date: January 2017
Valid through: January 2020
This activity is intended for clinical trial research physicians and nurses.
- Clinical trial addresses the tricky process of revealing genetic risk factors for Alzheimer’s
- Research on brain scan risk of Alzheimer’s an ethical challenge
- Best Practices Spotlight: An IRB chair’s job is never done
- When it was time to standardize, IRB went with a P&G committee
- IRB designs process to separate QI from research
- People with mental illness often excluded from clinical trials
- 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
Associate Editor: Dana Spector
Contributing Editor Melinda Young, Medical Writer Gary Evans, Editor Jill Drachenberg, Associate 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.
This course is no longer available to take.