Documentation Pain Management Groups Typically Request
Pain management and physical medicine practices often split procurement responsibilities between a medical director who signs off on which biologics categories the practice carries and an office manager who manages ordering and inventory. Before the first order, most groups ask for the donor eligibility summary and the sterility testing result tied to the specific lot, not just a general product data sheet.
Because physical medicine practices frequently carry both Wharton's jelly and exosome product lines, some ask Precision Biologics to supply separate documentation packets for each product family so records stay organized by type.
Bakersfield
NPPES registry listings, primary taxonomy, retrieved 2026-10-27
44- Pain Medicine
- 24
- Physical Medicine & Rehabilitation
- 20
Setting Up an NPI-Verified Account
An account is opened once a provider's NPI number is confirmed against the NPPES registry. For multi-provider pain management groups, each ordering physician typically verifies individually, which keeps lot-level traceability tied to the clinician who placed the order rather than to the practice as a whole.
Cold-Chain and Shelf-Stable Formats
Cryopreserved Wharton's jelly product ships overnight on dry ice and needs -80 degree Celsius storage on arrival; practices without that capacity sometimes choose the lyophilized Wharton's jelly or exosome formats instead, which are shelf-stable and stored per the instructions in that lot's product insert. Either way, the lot number should be logged into inventory as soon as the shipment is opened.
Medical Director Sign-Off
Confirming that a physical medicine or pain management practice's license and scope of practice support a particular product category is a decision for the practice's medical director and counsel, checked against the California medical board rather than against anything Precision Biologics publishes. Account setup includes a peer-to-peer call to walk through documentation, separate from any 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 multi-physician pain management group use one account for several providers?+
Yes, though each ordering physician's NPI is verified individually so lot-level records stay tied to the correct clinician.
What's the difference in storage requirements between product families?+
Cryopreserved Wharton's jelly formats require -80 C storage and overnight dry-ice shipping; lyophilized Wharton's jelly and exosome formats are shelf-stable per the product insert.
Does Precision Biologics publish pricing for pain management accounts?+
No. Pricing is available to verified accounts only, after NPI verification is complete.