Medical Director

Dr. Clay Buchanan, MD, provides medical oversight for Stem Nova Network: review of product documentation and training content, and oversight of our regulatory positioning.

  • FDA-Registered Facility
  • cGTP-Compliant (21 CFR Part 1271)
  • Dual-Lab COA Verified
  • NTA-Verified
  • USA Manufactured
Dr. Clay Buchanan, MD, Medical Director of Stem Nova Network

Dr. Clay Buchanan, MDMedical Director

About Dr. Clay Buchanan, MD

Dr. Buchanan is a board-certified family medicine physician trained at Texas Tech University Health Sciences Center, with a primary care background and more than 20 years of practice in Texas. He holds active medical licenses in Texas and Florida.

As Medical Director, he reviews Stem Nova Network's product documentation and training content for medical accuracy, oversees compliance with the regulatory frameworks that apply to our products, and checks that our materials stay within their classification.

His role is oversight and review. He does not practice medicine through Stem Nova Network, does not provide clinical recommendations to ordering practitioners, and does not direct patient care.

MDBoard certifiedFamily medicineLicensed in Texas & Florida20+ years in practice
  • RoleMedical Director, Stem Nova Network
  • TrainingTexas Tech University Health Sciences Center
  • SpecialtyFamily medicine; primary care background
  • LicensureTexas and Florida
  • FunctionQuality and compliance oversight, not clinical practice

Scope of the role

What the Medical Director does, and what sits outside the role.

Provides

  • Review of product documentation for medical accuracy
  • Review of training curriculum content
  • Oversight of compliance with 21 CFR Part 1271 standards
  • Evaluation of COA reporting standards
  • Guidance on regulatory framework interpretation

Outside the role

  • Clinical recommendations to ordering practitioners
  • Patient care decisions or protocols
  • Prescribing, ordering or directing product use
  • Endorsing products for any medical condition
  • Medical advice to patients or end users
  • Authorizing or credentialing practitioners

How oversight works

A quality and compliance function, applied before and after publication.

  1. Documentation review

    Product documentation and training materials are reviewed for medical accuracy, terminology and compliant positioning before release.

  2. Compliance monitoring

    Published materials are checked against 21 CFR Part 1271 positioning and for unsupported medical, disease or efficacy claims.

  3. Quality standard review

    Periodic review of COA reporting standards and testing documentation against our published quality claims.

What oversight checks

The standards our public materials are held to.

  • No approval impliedNothing implies FDA approval. hUCT-MSC products are individualized and not FDA-approved.
  • ClassificationExosome products are positioned as topical cosmetic products only.
  • No disease claimsNo disease-treatment, mechanism or efficacy claims.
  • Trust claimsFDA-Registered Facility, cGTP-Compliant, Dual-Lab COA Verified, NTA-Verified, State Licensed and USA Manufactured are checked against documentation.
  • ResponsibilityOrdering practitioners keep full responsibility for clinical decisions, patient care and informed consent. See our Medical & Legal Disclaimer.

Medical Director questions

More in the full FAQ.

Who is Stem Nova Network's Medical Director?

Dr. Clay Buchanan, MD, a board-certified family medicine physician trained at Texas Tech University Health Sciences Center, licensed in Texas and Florida.

What does the Medical Director review?

Product documentation, training content, COA reporting standards and compliance with the regulatory frameworks that apply to our products.

Does Dr. Buchanan give clinical guidance to ordering practices?

No. He does not provide clinical recommendations, patient care decisions, dosing or protocols. Clinical decisions remain with the licensed ordering practitioner.

Does medical oversight mean the products are endorsed for a condition?

No. Oversight is a quality and compliance function. It is not an endorsement of any product for any medical condition.

How do I raise a compliance or documentation question?

Use our contact page or your account representative.

Standards & science

Questions about our standards?

Our team can provide documentation, COAs and information about our oversight process.