THIS WEBINAR WILL EXPLAIN INSTITUTIONAL REVIEW BOA 2015 - Institutional Review Boards (IRBs): The Changing Landscape and the Effect on the Conduct of Clinical Research

Website http://bit.ly/1G010e8 | Edit Freely

Category Clinical Compliance;

Deadline: March 05, 2015 | Date: March 05, 2015

Venue/Country: Palo Alto, U.S.A

Updated: 2015-02-27 13:38:38 (GMT+9)

Call For Papers - CFP

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. Multi-site studies are becoming the standard.

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. She has initiated the planning, development, authorship and implementation of many human subjects’ research policies, practices, guidelines, submission and reviewer forms often working with state and federal authorities.

Use coupon code 232082 and get 10% off on registration.