A practical guide to running a compliant, audit-ready informed consent process, key ICF elements, re-consent rules, and common deficiencies.

Understand HIPAA's Privacy, Security, and Breach Notification Rules with a practical compliance checklist for clinics and providers.

Learn what Phase 4 clinical trials involve, why real-world evidence matters, and how TX/NM practices can start participating with support from TriStar CRC

Discover what happens in Phase 3 clinical trials, why they're called ‘pivotal,’ and how community practices in TX & NM can get involved.

Discover how Phase 2 clinical trials evaluate efficacy and optimize treatment. Learn what healthcare providers need to know about randomization, blinding, and site participation.

Discover how preclinical research tests safety and efficacy before human trials begin and what it means for the clinical trial pipeline.

Learn what Phase 1 clinical trials are, how maximum tolerated dose is determined, and why first-in-human studies are the foundation of drug development.

Discover how Site Management Organizations (SMOs) like TriStar CRC help private practices and clinics launch clinical trials—without building research infrastructure from scratch

Learn who does what in a clinical trial — PI, CRC, and CRA roles explained. Discover how private practices and specialty clinics can participate in clinical research with the right support.

Learn how clinical trial phases work. From preclinical to Phase 4 and how TriStar CRC helps providers and clinics become research sites with full support.

Learn what ALCOA-C means and why it matters for clinical research sites. Tristar helps providers build audit-ready, compliant research programs.

Learn how clinical research works with this guide, who the key players are, and how your practice can participate in clinical trials. TriStar helps sites get started with expert setup and full operational support.