Regulatory Guides

Good Clinical Practice: A Question & Answer Reference Guide 2024/2025 (Electronic)

Good Clinical Practice: A Question & Answer Reference Guide 2020/2021 (Electronic)

Good Clinical Practice: A Question & Answer Reference Guide 2020/2021

The Clinical Research Finance Roadmap: A Comprehensive Guide to the Financial Aspects of Clinical Research

The Clinical Research Finance Roadmap Companion Reference Guide: Tools, Templates and Resources (Electronic)

CRA Training Series: Volume 7 - Test Your CRA Knowledge (2018)

CRA Training Series: Volume 6 - The CRA's Reference for Adverse Events (2018)

CRA Training Series: Volume 5 - Conducting Routine Monitoring Visits (2018)

CRA Training Series: Volume 4 - Conducting the Study Initiation Visits (2018)

CRA Training Series: Volume 3 - Conducting the Prestudy Visit (2018)

CRA Training Series: Volume 2 - Identifying and Screening Investigators (2018)

CRA Training Series: Volume 1 - An Overview of Drug Development (2018)

CRA Training Series: A 7-Volume CRA Self-Study Curriculum (2018)

Study Site Training Series (2018): Volume 6: Understanding, Evaluating, and Implementing Clinical Protocols

Study Site Training Series (2018): Volume 5: Your Role in Reporting Adverse Experiences

Study Site Training Series (2018): Volume 4: Sponsor Visits and Regulatory Audits: What You Need to Know

Study Site Training Series (2018): Volume 3: IRBs/IECs and Informed Consent: Protecting the Rights of Human Subjects

Study Site Training Series (2018): Volume 2: FDA Clinical Research Regulations and GCPs: The Essentials

Study Site Training Series (2018): Volume 1: The Clinical Study Site Team: Roles and Responsibilities

Study Site Training Series (2018): A 6-Volume Self-Instructional Training Series for Investigative Teams

The Form FDA 1572: A Reference Guide for Clinical Researchers, Sponsors, and Monitors

Good Clinical Practice: A Question & Answer Reference Guide 2026/2027

Good Clinical Practice: A Question & Answer Reference Guide 2026/2027 (Electronic Edition)