Institutional Review Boards (IRBs): The Changing Landscape and the Effect on the Conduct of Clinical Research

This clinical research training will explain the Institutional Review Board (IRB) models. It will discuss the regulatory framework for IRB review including 21 CFR 50, 56 and 45 CFR 46.

Why Should You Attend:

The number of clinical trials continues to increase. Clinical trials are no longer solely conducted at academic research centers or hospitals. Stand-alone facilities set up to conduct research are being established. Partnerships are being formed between traditional centers and the community. 

Who Will Benefit:

Clinical Quality Assurance Professionals

Clinical Research Associates,

Project Managers, or others involved in site and IRB assessment Clinical Investigators

Study Coordinators

IRB Members IRB Professionals

Clinical Research Coordinator

Instructor Profile:

Dr. Sarah Fowler-Dixon, PhD, CIP is Education Specialist and instructor with Washington University School of Medicine. She has developed a comprehensive education program for human subject research which has served as a model for other institutions. She crafted budgets, policies, procedures, reporting, and training for the new program.

Note:

Use coupon code NB5SQH8N and get 10% off on registration.

For Registration:

http://www.complianceonline.com/institutional-review-boards-irbs-changing-requirements-webinar-training-703400-prdw?channel=sciencedz