Whole-person care, on your schedule, under consented protocols.
See a U.S. licensed physician by phone or video. Access consented regenerative medicine, research and investigational therapies, and consented TOL oleander treatment, with a 16-year manufacturing record and 19,000-plus subjects served in research and investigational settings.
Three pathways. One coordinated team.
Every pathway runs on signed informed consent, physician supervision, and a complete chain of custody from manufacturer to patient.
WJ Exosome, Home IV, and Topicals
Wharton's jelly derived exosome therapy, in-home IV infusions, and topical formulations. Each lot is paired with a cGMP Certificate of Analysis and a chain of custody log from the U.S. manufacturer to the bedside.
- Telemedicine evaluation
- Disease-specific consent
- Lot and batch traceability
- RN home administration
IRB-supervised access pathways
Participate in IRB-overseen research and investigational protocols delivered through TRM Health. All therapies referenced here are investigational and are not FDA-approved to treat any specific disease or condition.
- IRB-approved protocols
- Adverse event monitoring (MedWatch ready)
- De-identified outcome reporting
- No guarantee of clinical benefit
TOL Protocol, oral and IV
TOL Protocol is a consented research and investigational use of oleander-derived material under physician supervision. Patients sign a TOL-specific informed consent that explains potential cardiac risks, contraindicated medications, and the strictly investigational nature of the therapy.
- TOL-specific informed consent
- Cardiac risk and drug interaction screening
- Oral and IV protocols
- Continuous physician oversight
From first call to coordinated care in four steps.
Request a visit
Sign in and book a phone or video visit. Intake is conditional and only collects what your protocol requires.
Sign your consent
Review and sign the disease-specific consent (WJ Exosome, TOL, Home IV, Topicals) and the Texas 22 TAC 171.2(b) form where applicable.
Meet your physician
Encounter is documented in real time. AI drafts a SOAP note. Your physician reviews, edits, and countersigns it.
Treatment delivered
Verified cGMP lot ships cold-chain to your home, or an RN performs the visit. You see every step in your portal.
16 years of cGMP biologic manufacturing. 19,000-plus subjects supported.
TRM Health partners with a U.S.-based cGMP manufacturer with a 16-year operating record and a documented experience base of more than 19,000 subjects served across research and investigational service settings. Every shipment carries a lot Certificate of Analysis and a tamper-evident chain of custody log.
Therapies and protocols described on this page are investigational. They are not FDA-approved to diagnose, treat, cure, or prevent any disease. See the full disclaimers.
Read full disclaimersBuilt for clinicians, regulators, and the patients they serve.
Answers, in plain language.
Ready to talk to a physician?
Same-week scheduling for most consented protocols.