Informed Consent Made Simple - Forms, Purpose, and Practice in Clinical Research

A Comprehensive Guide to What Patients and Families Need to Know and What Professionals Must Understand

If you work in clinical research, you know that informed consent is more than a form.
It’s the foundation of trust between participants and professionals.

This book provides a clear, step-by-step guide to understanding the purpose, process, and practice of informed consent in modern clinical research.
You’ll learn how to communicate complex information clearly, protect patient rights, and ensure ethical standards in every study.

Inside, you’ll find:
• How informed consent evolved and why it matters today
• The legal and regulatory frameworks guiding research ethics
• Core elements every consent form must include
• How to write in plain language for accessibility and understanding
• Real-world examples of effective consent discussions

You’ll explore:
• Common challenges and controversies in consent
• How to strengthen communication between sites and participants
• Tools and resources for patients, families, and professionals
• The future of informed consent, from eConsent to AI-assisted communication
Each chapter offers practical insights, ethical perspectives, and actionable strategies to improve the consent process across all trial phases.
This book is for:
• Patients, families, and caregivers who want to better understand their rights
• Clinical research professionals and investigators
• Regulatory and ethics specialists
• Anyone who supports and values transparency in clinical research


If your work or decisions involve clinical trials, Informed Consent Made Simple is the comprehensive guide you’ve been waiting for. Order your copy TODAY!