HIS TRAINING ON CLINICAL STUDY DEVIATIONS WILL HEL 2015 - Deviations: What are they? Do you need to report?

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Category Clinical Compliance;

Deadline: February 24, 2015 | Date: February 24, 2015

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

Updated: 2015-02-20 15:17:14 (GMT+9)

Call For Papers - CFP

Why Should You Attend:

As the human subjects regulatory framework continues to grow and be further defined, it is important to know when and what needs to be submitted, reviewed, and approved by an Institutional Review Board (IRB) prior to implementation by the study team. Alternatively, as studies become more complex and complicated the study team often has to make immediate decisions which may not allow time for a regulatory consult.

Who Will Benefit:

This webinar will provide valuable assistance to all personnel in:

Human Subjects Research

Healthcare interested in exploring the field of Clinical Research

New Clinical Research Coordinator positions (1-2 years)

New Principal Investigator positions

Instructor Profile:

Dr. Sarah Fowler-Dixon,PhD, CIP has presented on various human subjects topics since 2001 at local, regional, and national conferences. She developed a comprehensive education program for human subject research which has served as a model for other institutions.

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