For doctors & providers

Advanced support, documentation,
protocols and product access.

In partnership with our outside medical board, we have launched IORE, our dedicated educational platform created to support you well beyond your initial order.

IORE is designed to be your go-to resource as you integrate and scale biologic applications within your practice.

Apply for provider access

Patient referral network

Patients who request information through this site are routed to a participating provider by ZIP code. Providers control whether they receive referrals, and a single provider may hold a ZIP exclusively.

Routing

By ZIP code

Enquiries are matched to the provider covering that ZIP. Two providers in the same ZIP share them evenly, round-robin.

Exclusivity

$1,500/month

Hold a ZIP outright and take every enquiry from it. Available on request from your provider portal.

On joining

Nothing is wasted

Enquiries already received for your ZIP before you joined are attached to your account when you activate referrals.

Clinical modules

Descriptions below are reproduced from our clinical education material.

Module

How do we talk to patients about “Stem Cells”?

When presenting human cell and tissue products (HCTPs) to patients, providers should avoid unregulated terms like “stem cells” and instead focus on tissue-specific supplementation for cartilage-based defects, explaining that these products supply collagenic growth factors (like type I, II, and III collagen) that may help the body heal itself at a cellular level—especially when inflammation is controlled. By using FDA-aligned language, discussing patient-specific regenerative capacity, and matching graft complexity to injury severity and age, clinicians can ethically and effectively guide patients through their options.

Module

Regulatory Environment Around Stem Cells — Dispelling Myths

Dr. Martin delivers a critical and detailed overview of the U.S. regulatory landscape surrounding stem cells, emphasizing that using the term “stem cells” in clinical practice is scientifically inaccurate and legally risky. He explains that current compliant use involves human cell and tissue products (HCTPs) like Wharton's Jelly, which are structural allografts meant to supplement local cartilage defects—not regenerate tissue or treat systemic diseases like osteoarthritis, which would constitute unapproved drug claims.

Module

Are Stem Cells a Scam?

Dr. Martin addresses the misconception that “stem cells” are a cure-all, emphasizing that successful regenerative outcomes depend not on magical products but on proper clinical application rooted in scientific understanding—especially of collagenic differentiation. He urges providers to move beyond marketing hype, deepen their knowledge of biologic mechanisms, and practice evidence-based medicine if they want to stay competitive and deliver meaningful patient results.

Module

The basics behind Allogeneic Science

Dr. Martin offers a science-based explanation of how allografts—particularly Wharton's Jelly—contribute to structural support and localized tissue optimization through collagenic signaling. He encourages providers to move beyond the outdated “stem cell” terminology and focus on the well-characterized growth factor profiles found in structural tissue allografts. Dr. Martin also underscores the importance of using these materials within defined, localized applications and cautions against making non-compliant claims related to systemic effects or disease reversal.

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Full modules, protocols and documentation are available to registered providers.

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Important: This content is provided for educational purposes and research use only (RUO). It reflects the professional experience and academic perspectives of credentialed providers and is not intended to diagnose, treat, cure, or prevent any disease. Clinical application and regulatory compliance remain the responsibility of the licensed provider.