Documentation pain management practices typically request
Multidisciplinary pain and physical medicine groups generally request supplier documentation before adding a biologics line to their sourcing options: a certificate of analysis tied to lot number, a donor eligibility summary, and confirmation of third-party sterility testing and quarantine release.
Because these practices often order smaller volumes on a rolling basis compared to surgical groups, consistent lot-level traceability through to the patient record is usually weighted heavily in vendor selection.
Springfield
NPPES registry listings, primary taxonomy, retrieved 2026-10-27
27- Pain Medicine
- 15
- Physical Medicine & Rehabilitation
- 12
Account verification and ordering access
Access to order is gated by NPI verification, which confirms the requesting account belongs to a licensed physician or a practice operating under physician supervision. This applies equally to solo pain management providers and larger physical medicine groups.
Precision Biologics does not publish pricing. Verified accounts receive pricing and lot availability directly.
Cold-chain delivery into the Northeast
Cryopreserved inventory is held at -80 degrees Celsius and shipped overnight on dry ice in validated containers after an order is placed, with recovery-to-processing completed within 48 hours upstream of storage. A pain management office receiving its first shipment should confirm someone is on site to accept a dry-ice package rather than routing it through a general mailroom.
Confirming regulatory posture with counsel
Whether a particular intended use of a Wharton's jelly or exosome product falls within the supplier's 361 HCT/P framework or is instead regulated as a biologic drug is a determination for the practice and its own counsel, not something Precision Biologics certifies on a practice's behalf. Massachusetts-based groups should raise scope and supervision questions directly with the Massachusetts medical board.
Support on the Precision Biologics side includes peer-level calls between physicians to walk through documentation, plus registration and licensure records available to verified accounts 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 solo pain management provider in Springfield open an account?+
Yes. Account access is based on NPI verification, not practice size, so solo providers and group practices are evaluated the same way.
Does Precision Biologics recommend which product fits a given procedure?+
No. The supplier provides documentation and logistics support only. Clinical and procedural decisions, including which product to use, remain with the treating physician.
What happens if a shipment arrives and no one is available to accept it?+
Because cryopreserved products ship on dry ice in validated containers, practices should confirm delivery scheduling and staff availability before their first order.