HomeAbout UsContact Us
Advanced Search
All CoursesCourses by TopicCourses by SpecialtyCourses by Specialty CreditRegister Now!!
Register Now!!
Member Login
Your Account
Your Test History
Your Certificates
Your Payment History
All Courses
Courses by Topic
Courses by Specialty
Courses by Specialty Credit
Accreditation
State Requirements
FAQs
 
Home : Advanced Search : Course view :






Course: IRB Advisor 1603 


Specialty: Clinical Trial Research Format: Text 
Course #: 10393  Price: $15.00  
Release date: 2012-03-01  Valid through: 2015-03-01  
Publication: This activity originally appeared in IRB Advisor (CME). 
Course viewing requirements (opens in a new window)
Instructions for Course Participation (opens in a new window)
Legal disclaimer (opens in a new window)


Target Audience:
This activity is intended for clinical trial research physicians and nurses.
Sponsor:
This activity is sponsored by AHC Media.
Accreditation:
AHC Media is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.
Credit Designation:
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.
Faculty
Editors
Suzanne Koziatek
Melinda Young

Associate Managing Editor
Jill Von Wedel
AHC Media

Nurse Planner
Kay Ball, RN, PhD, CNOR, FAAN
Perioperative Consultant/Educator
K & D Medical
Lewis Center, OH

Physician Reviewer
Mark S. Schreiner, MD
Associate Professor of Anesthesia in Pediatrics
University of Pennsylvania Chair
Committee for the Protection of Human Subjects
The Children's Hospital of Philadelphia


Subjects:
  • IRB offices face staffing changes as leaders age
  • Career tracks can benefit any size office
  • Create "recipes" of job roles
  • Study suggests need for more clarity in IC process
  • Presidential commission promotes reforms
  • Improving access, ethics
  • Audit toolbag puts focus on improvement
 
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
 
Financial Disclosure:
Editor Suzanne Koziatek, Editor Melinda Young, Associate Managing Editor Jill Von Wedel, Nurse Planner Kay Ball, RN, PhD, CNOR, FAAN, and Physician Reviewer Mark S. Schreiner, MD, report no consultant, stockholder, speaker's bureau, research, or other financial relationships with companies related to the content in this CNE/CME activity.

Copyright 2012 AHC Media. All rights reserved.
 
  • You are not currently logged in.
  • To view content articles and complete the post-test for this course, please login or register now

 



Copyright Notices  | Terms of Use  
Privacy Statement