What documentation to request
Before adding a tissue or extracellular vesicle product, pain management and physical medicine groups commonly request lot-specific documentation rather than general marketing claims.
These records are available to verified accounts on request, and we do not publish composition or concentration figures beyond what is stated on a lot's own certificate of analysis.
- Certificate of analysis for the specific lot
- Donor eligibility summary
- Lot release record confirming completed sterility testing and quarantine release
San Antonio
NPPES registry listings, primary taxonomy, retrieved 2026-10-27
326- Pain Medicine
- 140
- Physical Medicine & Rehabilitation
- 186
Medical director review and licensure
Every account requires NPI verification, and we recommend the supervising physician or medical director review product documentation before a practice's first order. We also recommend confirming your practice's purchasing policy with the Texas Medical Board and your own counsel, since our registration as a distributor does not replace a practice's internal review process.
Receiving shipments in South Texas
Cryopreserved lots are stored at -80 degrees C and ship overnight on dry ice in validated containers, so a staffed receiving window matters for practices taking delivery in San Antonio. Lyophilized formats are shelf-stable without cryogenic storage, which some practices prefer for simpler receiving.
Each lot ships with a unique identifier so the receiving practice can log use at the patient record level for its own compliance purposes.
Opening an account with us
A practice manager can typically start the intake process, and Precision Biologics supports account setup through access to physician-level conversations about documentation, not clinical advice. Once NPI verification and medical director review are complete, most San Antonio pain management and physical medicine accounts are ready to place a first order.
FDA has stated there are no FDA-approved exosome products. Exosome products are generally regulated as biologic drugs under section 351 of the Public Health Service Act, not as 361 HCT/Ps. Purchase and clinical use decisions belong to the physician with their own regulatory counsel.
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
Do you distinguish between pain management and physical medicine practices for account setup?+
No. Both are eligible for a verified account as long as the practice is licensed and has a valid NPI number on file.
What logistics should our San Antonio practice plan for with cryopreserved shipments?+
Cryopreserved products ship overnight on dry ice in validated containers and require storage at -80 degrees C on arrival, so a staffed receiving window should be in place before the first order ships.
Who at our practice should review the product documentation before we order?+
We recommend the supervising physician or medical director review the certificate of analysis, donor eligibility summary, and lot release record before the practice opens an account.