Guiding Principles in Clinical Research: The Essentials (GCP, Informed Consent, and Quality Assurance) - Charles Mackay, PhD

↳ This is a section part of Moment: CRT 2016 Atherosclerosis & Research - How to Build a Successful Clinical Research Program: Part I

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Summary

Guiding Principles in Clinical Research: The Essentials (GCP, Informed Consent, and Quality Assurance) presented by Charles Mackay, PhD at CRT 2016

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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: Part I

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 - Louis Cannon, MD, FSCAI, FACC
What Are the Essentials to Run a Large Research Organization? - A. Michael Lincoff, MD
Guiding Principles in Clinical Research: The Essentials (GCP, Informed Consent, and Quality Assurance) - Charles Mackay, PhD
How Does the IRB Function and How to Get Approval for the First Time - Priscilla Adler, MBA, CCRP
Ethics of Human Subjects Research - Charles Mackay, PhD
FDA Audits - Kate Dalton, MS, RD, CCRC
Investigator-initiated Research: What Are Your Responsibilities? - Roxana Mehran, MD, FACC, FSCAI
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