Clinical Research Compliance & Regulatory Consulting
Tru Research specializes in ClinicalTrials.gov compliance, informed consent development, and protocol writing compliance — helping research teams navigate complex regulatory requirements with confidence.
"We go beyond checking boxes — our mission is to build trust in research, ensure integrity, and advance discoveries that improve lives."
— Anita Trupiano, Founder & Principal Consultant, Tru Research
Our Expertise
We work with investigators, research institutions, and sponsors to ensure studies meet regulatory standards — protecting both data integrity and participant safety.
Study registration, results reporting, and PRS (Protocol Registration and Results System) navigation, handled start to finish.
IRB and FDA-compliant informed consent documents, written to meet regulatory standards while staying clear for participants.
Structuring study protocols to meet IRB, FDA, and ICH-GCP standards from the outset.
Why Tru Research
Anita Trupiano has spent over a decade in clinical research — as a research coordinator, site director, and now Program Development Analyst & Regulatory Affairs Specialist at Rutgers Cancer Institute of New Jersey. That's given her a working knowledge of research compliance from every seat at the table: coordinating IRB submissions, running ClinicalTrials.gov reporting, and building hospital research programs from the ground up.
View Career History →Interested in collaborating, or need compliance support for your study? Reach out to discuss how Tru Research can support your clinical research needs.
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