FDA Audits - Kate E. Dalton, MS, RD

↳ This is a section part of Moment: CRT 2015 Atherosclerosis & Research - How to Build a Successful Clinical Research Program

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Summary

FDA Audits presented by Kate E. Dalton, MS, RD at CRT 2015

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Target Audience

  • Interventional Cardiologists
  • Interventional Fellows
  • Physiology technicians
  • Nurses and other allied healthcare professionals 

Session Name: How to Build a Successful Clinical Research Program

Track: Atherosclerosis & Research

Learning Objectives

  • The latest updates in Atherosclerosis and the Essentials of Clinical Research

Other Components in this Moment

Overview
Building and Maintaining a Sound Clinical Research Program - Alexandra J. Lansky, MD
The Role and Expectations of a Research Coordinator - Michelle Deville, RN
What Are the Essentials to Run a Large Research Organization? - Donald E. Cutlip, MD
Guiding Principles in Clinical Research: The Essentials (GCP, Informed Consent, and Quality Assurance) - Charles R. Mackay, PhD
How Does the IRB Function and How to Get Approval? - P. N. Adler, MBA, CCRP
FDA Audits - Kate E. Dalton, MS, RD
Investigator-Initiated Research: What Are Your Responsibilities? - Roxana Mehran, MD
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