Clinical Trial Resources
Dive into our curated collection of resources for clinical trial participants and organizations running or sponsoring trials. The links below lead to pages that provide answers, guidance, and actionable insights.
For Participants
These resources aim to educate and support individuals considering or participating in clinical trials:
​
A comprehensive database of publicly and privately supported clinical studies conducted around the world.
​
FDA Clinical Trials Information
Guidance on participant safety, informed consent, and the role of the FDA in clinical research.
​
Center for Information and Study on Clinical Research Participation (CISCRP)
Educational resources and a searchable database of trials to help participants make informed decisions.
​
Coalition of Patient Advocacy Groups
Patient-focused organizations that can help connect participants with relevant trials and offer peer support.
​
Explore DHN's comprehensive Clinical Trial FAQs to learn about trial types, compensation, safety protocols, and more.
For Organizations Running or Sponsoring Clinical Trials
These resources help organizations streamline operations, ensure compliance, and improve participant engagement:
​
ICH Good Clinical Practice (GCP) Guidelines
Internationally recognized standards for clinical trial conduct.
​
Regulatory guidance documents on clinical trial design, execution, and reporting.
​
NIH’s Inclusion Across the Lifespan Policy
Best practices for recruiting diverse participant populations, ensuring trials are representative.
​
Clinical Data Interchange Standards Consortium (CDISC)
Standardized frameworks for collecting and reporting trial data.
​