Clinical Trials Audit Preparation – A Guide for d Clinical Practice (GCP) Inspections

VERA MIHAJLOVIC-MADZAREVIC has more than twenty years of experience in scientific and clinical research in the academia and industry. She is the Director of Global Research Pharma Canada. She conducts Good Clinical Practice (GCP) audits for the pharmaceutical, biotech, and medical device industries worldwide in compliance with FDA, Health Canada, and other regulations. She also trains clinical and scientific personnel in GCP and clinical research, leading the Training and Professional Development Programs at the Clinical Research Institute of America (criamerica.com) and the Academy of Applied Pharmaceutical Sciences.

Preface. Introduction: Background History on Clinical Standards. Glossary. Chapter 1. Good Clinical Practice and Therapeutic Product Development. 1.1 Good Clinical Practice in Clinical Research. 1.2 Role of the Sponsor of a Clinical Investigation. 1.3 Role of the Institutional Review Board/Independent Ethics Committee (IRB/IEC). 1.4 Roles and Responsibilities of the Clinical Trail Investigator. 1.5 Clinical Trial Protocol and Protocol Amendments. Chapter 2. Therapeutic Products Clinical Development in the United States. 2.1 Drug Discovery. 2.2 Preclinical Development. 2.3 Clinical Development. 2.4 FDA Considerations for Drug Development. 2.5 Phase IV, Postmarketing Surveillance and GCP. 2.6 Quality Assurance in Clinical Research. 2.7 FDA Inspectional Background and Data. 2.8 DFA Bioresearch Monitoring Program. Chapter 3. The Inspection Preparation. 3.1 Conduct of an Internal GCP Inspection: Quality Assurance Inspection. 3.2 Steps to Prepare for the Internal QA Inspection. 3.3 The GCP Quality Assurance Unit. 3.4 Steps to Prepare for the Regulatory Inspection. 3.5 Clinical Investigator Inspections Preparation. 3.6 What to Do When an Investigator Site FDA Inspection is Announced. 3.7 Sponsor's Inspection Preparation. 3.8 What to Do When Sponsors FDA Inspector Arrive Unannounced. 3.9 The Institutional Review Board Inspections Preparation. 3.10 What to Do When an IRB FDA Inspection is Announced. 3.11 The Investigator Site Inspection. 3.12 Investigator's Responsibilities. 3.13 Types of Clinical Investigator Site Inspections. 3.14 Inspectional Procedures. 3.15 FDA Audit Procedures for Investigative Sites. 3.16 FDA Inspections of International Clinical Trial Sites. 3.17 The Audit Report and Form. Chapter 4. Analysis of Warning Letters. 4.1 Analysis of Warning Letters Issued to Clinical Investigators. 4.2 An Analysis of Warning Letters Issued to Clinical Trial Sponsors. 4.3 Analysis of Warning Letters Issued to Institutional Review Boards. Chapter 5. Fraud and Misconduct in Clinical Research. 5.1 What Type of Data is Falsified? 5.2 How is Data Falsified? 5.3 Why is Data Falsified? 5.4 Who Falsified the Data? 5.5 What Can be Done to Detect Fraud? 5.6 How Do We Prevent Fraud? Appendix A. Some Answers to the Most Problematic Questions in Compliance. Appendix B. Guidance for Industry-E6 Good Clinical Practice: Consolidated Guidance. Appendix C. World Medical Association Declaration of Helsinki Ethical Principles for Medical Research Involving Human Subjects. Appendix D. Nuremberg Code. Appendix E. The Belmont Report: Ethical Principles and Guidelines for the Protection of Human Subjects of Research. Index.