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Education & Resources

Access a collection of trusted resources designed to help you better understand clinical research, patient rights, and the processes behind modern medical studies. Whether you’re considering participation or simply looking to learn more, these materials provide clear, reliable information to guide you.

Clinical Research:
The Basics

national institute of health logo

An easy-to-understand overview of clinical trials, including how they work, the different types of studies, and what to expect as a participant. A great starting point for anyone new to clinical research.

USDHHS:
Belmont Report

A foundational guide to the ethical principles behind clinical research, focusing on protecting participants through respect, safety, and fairness. It outlines the core standards that ensure studies are conducted responsibly and with patient rights in mind.

Drug Developement Process

U.S Food and drug administration

An overview of how clinical research is conducted, including the different phases of trials and how treatments are tested for safety and effectiveness before approval. It helps explain how new therapies move from research to real-world use.

The Nuremburg Code: Directives For Human Research

the office of research integrity logo

A historic set of ethical guidelines that established the foundation for human subject research, emphasizing voluntary consent, safety, and the responsibility to protect participants. It remains a cornerstone of modern clinical research standards. 

Informed Consent

U.S Food and drug administration

An overview of the informed consent process in clinical research, explaining how participants are given clear, complete information about a study before agreeing to take part. It highlights the importance of transparency, patient understanding, and protecting individual rights.

Declaration of Helsinki

world medical association logo

A globally recognized set of ethical principles for medical research involving human participants, focused on protecting patient rights, safety, and well-being. It guides how clinical studies are conducted with integrity and respect for individuals. 

FDA:
Good Clinical Practice

U.S Food and drug administration

An overview of the regulations and standards that govern how clinical trials are conducted, ensuring studies are designed, monitored, and reported properly. These guidelines protect participant safety while ensuring the data collected is accurate and reliable.

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