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

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

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Summary

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