Verify your standing before you order
Before placing an order, Indiana clinics should confirm their own standing with the Indiana Medical Licensing Board and, for medspa locations, document the physician medical-director and supervision structure that applies to the services offered there. Clinics should also check with the relevant state pharmacy or health facility licensing authority about any requirements for receiving and storing biologic products, and should route the intended use of a given product past their own healthcare counsel.
Precision Biologics does not provide legal advice and does not advise on clinical use, dosing, or procedure protocols. Documentation such as certificates of analysis, donor eligibility summaries, and lot release records is available on request to support that internal review.
NPI-verified accounts and cold-chain delivery
Opening an account starts with NPI verification; Precision Biologics confirms the requesting practice's National Provider Identifier against the NPPES registry before any order is processed. Once an account is approved, cryopreserved products ship overnight on dry ice in validated containers directly to the clinic, and lyophilized formats ship at ambient temperature per the product insert.
Every lot carries a unique identifier so the receiving clinic can track use at the patient-record level on its own side. Staff can also request a peer-to-peer call with a Precision Biologics contact to review documentation questions - these calls address paperwork and sourcing, not clinical decisions.
Indiana clinics by registry count
Precision Biologics sees interest from orthopedic, pain management, and aesthetic/medspa practices across Indiana, with the heaviest concentration of licensed providers located in Indianapolis, Fort Wayne, and South Bend. Public NPPES registry data for these three cities shows approximately 365 providers under orthopedic taxonomies, 313 under pain management, and 212 under aesthetic-related taxonomies.
These figures are registry counts for the named cities only - not a statewide total, not a measure of active buyers, and not an endorsement by any licensing body. Clinics should treat them as a general reference point rather than a market claim.
These products are not FDA approved or licensed for any disease or condition. Information is for licensed healthcare professionals and is not medical or legal advice.
Frequently asked questions
Does Precision Biologics sell directly to patients in Indiana?+
No. Accounts are limited to licensed physicians, orthopedic and pain practices, and physician-supervised medspas with a verified NPI. Patients should direct product questions to their treating clinic.
What documentation can an Indiana clinic request before purchasing?+
Clinics can request a certificate of analysis, donor eligibility summary, and lot release record for a given lot. Full ingredient disclosures for exosome products are provided to verified accounts.
Are Wharton's jelly and exosome products FDA approved?+
No FDA-approved exosome products exist, and Wharton's jelly allografts are not FDA approved or licensed for any disease or condition. Clinics should confirm the regulatory posture of a specific intended use with their own counsel.