Release date: April 2017
Valid through: April 2020
This activity is intended for clinical trial research physicians.
- A fresh method to adverse event tracking in behavioral studies
- No ROMP in the park: The complex intersection between QI and clinical research
- Ethical issues of recruiting research participants via social media
- Highlights from social media research recruitment checklist
- Jazz up educational materials with infographics
- One IRB’s compliance improvement strategies in a nutshell
- A consent consult helps new researchers with informed consent
- Student receives IRB approval to collect and display comments from sexual assault victims
- 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
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.