For Physicians
If you are running an innovative therapy in your practice, your patients are your evidence base. Beacon turns that evidence into something the world can cite.
Why physicians work with us
You went into medicine to help patients, not to wrestle with IRB submission templates and ClinicalTrials.gov PRS account flags. We built Beacon because we spent fifteen years doing exactly that — and we know the shortcuts.
Our founder, Tamara C Tamas, holds an MS in Biopharmaceutical Regulatory Affairs and is Principal Investigator on multiple ClinicalTrials.gov-registered observational studies. Every study we register uses Tamara (or a similarly credentialed colleague at Healing Hope International) as the PI of record — so you get full regulatory coverage without having to become a regulatory expert yourself.
Who this is for
Regenerative medicine clinics (stem cell, PRP, exosome, peptide therapy)
Functional and integrative medicine practices with proprietary protocols
Neurological rehabilitation and brain-injury recovery programs
Orthobiologic and sports-medicine specialists
IV therapy, HBOT, and longevity medicine clinics
Any licensed provider delivering an innovative therapy that warrants outcome tracking
What you get
A real clinical protocol
Not a template. We interview you, shape the observational design around your practice, and hand you a document an IRB will actually approve.
ClinicalTrials.gov NCT number
Your study listed publicly, searchable by patients and payers alike. Typical turnaround: 4–6 weeks from kickoff.
Patient enrollment portal
Branded, mobile-first. Electronic informed consent. Validated questionnaires delivered on the schedule your protocol specifies.
Functional-status tracking
PROMIS, FIM, WOMAC, condition-specific instruments — we pick the right ones and handle the licensing.
Publication-ready data
Quarterly analyses, manuscript outlines, abstract support. Your registry becomes a paper; your paper becomes awareness for the therapy.
What it is not
We do not run interventional trials with drug regulators, FDA INDs, or phase-I dose-escalation studies. If you need that, you need a full CRO, and we will tell you so.
We do not tell you what to treat or how to treat it. The clinical judgment stays with you. We are the people who wrap your existing practice in rigorous observational methodology so the data you generate is credible, usable, and publishable.
We do not charge per enrollee, per data point, or per-publication. Flat setup fee, flat monthly. Add-ons priced clearly.
Ready to start?
The intake form takes ten minutes. A member of our team will respond within one business day with a scoped protocol summary and a fixed-fee quote.