Documentation pain management practices typically request
Before adding a biologics vendor, pain management and physical medicine practices generally ask for the same baseline paperwork: a certificate of analysis for the lot, a donor eligibility summary describing the screening process, and confirmation of third-party sterility testing results.
Precision Biologics makes this documentation available to verified accounts, along with a lot release record confirming that quarantine and internal release criteria were met before shipment.
Atlanta
NPPES registry listings, primary taxonomy, retrieved 2026-10-27
247- Pain Medicine
- 106
- Physical Medicine & Rehabilitation
- 141
Account setup and NPI verification
Because orders are restricted to licensed professionals, account setup confirms an active NPI number and practice information before the first order ships.
Shipping and storage across the Southeast
Cryopreserved Wharton's jelly products ship overnight on dry ice in validated containers and require storage at -80 degrees Celsius on arrival. Lyophilized exosome and Wharton's jelly formats are shelf-stable and ship without cryogenic packaging, with storage and reconstitution handling described in the product insert.
A pain management practice receiving either format should log the lot number on arrival and retain it for patient-record-level traceability, consistent with how the supplier tracks each lot.
Verifying regulatory standing
Precision Biologics does not determine whether a given intended use meets the minimal manipulation or homologous use criteria in 21 CFR 1271.10, and we do not provide dosing or procedure guidance. Atlanta practices should confirm their regulatory posture with the Georgia medical board and their own counsel.
Our team can arrange peer-to-peer calls between physicians to review product documentation; these calls address specifications, not clinical decision-making.
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
Can a pain management clinic in Atlanta open an account without an NPI number?+
No. Account verification requires an active NPI number tied to a licensed practice or physician.
Do you provide dosing or injection protocols for pain management use?+
No. We do not advise on dosing, procedures or clinical protocols. Those decisions belong to the treating physician.
What is the difference between the cryopreserved and lyophilized formats you distribute?+
Cryopreserved formats require -80 degree Celsius storage and overnight dry-ice shipping. Lyophilized formats are shelf-stable and do not require cryogenic storage; handling instructions are in the product insert.