Documentation a pain management practice should request
A pain management or physical medicine practice evaluating a new biologics vendor typically asks for the same baseline documents regardless of the vendor's size or region: a lot-specific certificate of analysis, a donor eligibility summary, and a plain description of recovery, testing, and release criteria. Requesting this paperwork up front, before the first order, is the more common approach among practices with an established vendor-review process.
This documentation set is available to verified accounts and can be reviewed with a practice's compliance contact on request.
Killeen
NPPES registry listings, primary taxonomy, retrieved 2026-10-27
21- Pain Medicine
- 16
- Physical Medicine & Rehabilitation
- 5
NPI verification before ordering
An NPI number verified through the NPPES registry, the same source behind the Pain Medicine and Physical Medicine & Rehabilitation counts above, is required before an account can place an order. The process applies equally whether the practice is in Killeen or elsewhere.
Each lot is logged against the account so the practice's own traceability records can be reconciled with what it received.
Cold-chain shipping to Central Texas
Cryopreserved products are stored at -80 degrees C and ship overnight on dry ice inside validated containers, a path that reaches Killeen the same way it reaches other destinations in the Southwest. Lyophilized exosome and Wharton's jelly formats are shelf-stable and follow the handling instructions included with the specific lot rather than requiring cold-chain receiving.
Designating a staff member to receive and log a cryopreserved shipment the day it arrives keeps the product within its intended storage window.
State verification and account setup
Exosome products have no FDA approval; FDA has stated there are no FDA-approved exosome products and that they are generally regulated as biologic drugs, so purchase and clinical-use decisions belong to the treating physician and their own counsel. Wharton's jelly products are offered under the supplier's HCT/P framework, and whether a given intended use satisfies 21 CFR 1271.10 is a determination for the practice and its counsel, not Precision Biologics.
Practices should verify their own standing with the Texas Medical Board directly. Account setup itself involves NPI confirmation, basic practice details, and a documentation review, with a peer-level conversation about that paperwork available on request.
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 physical medicine and rehabilitation practice in Killeen open the same type of account as a pain medicine practice?+
Yes. Both specialties go through the same NPI verification and documentation review, and neither is treated differently during account setup.
Is there a minimum order size for a Killeen-based practice?+
Order details, including minimums, are shared with accounts once NPI verification is complete rather than published generally.
What should we verify before purchasing an exosome product for our practice?+
Confirm your own standing with the Texas Medical Board and your legal counsel, and review the documentation Precision Biologics provides, since exosome products are not FDA approved and purchase decisions rest with the physician.