Documentation pain and physical medicine practices typically request
Before adding any tissue or extracellular vesicle product, pain management and physical medicine groups commonly ask a distributor for lot-specific records rather than general marketing material.
Precision Biologics provides these records on request to verified accounts and does not publish composition or concentration data beyond what appears on the lot's own certificate of analysis.
- Certificate of analysis for the lot
- Donor eligibility summary
- Lot release record confirming quarantine and sterility testing were completed
Charlotte
NPPES registry listings, primary taxonomy, retrieved 2026-10-27
169- Pain Medicine
- 56
- Physical Medicine & Rehabilitation
- 113
Shipping and receiving for Southeast practices
Cryopreserved products are shipped overnight on dry ice in validated containers after storage at -80 degrees C, while lyophilized formats are shelf-stable without cryogenic storage. Charlotte practices receiving cryopreserved lots should plan for a staffed delivery window so the product moves directly from the carrier into proper storage.
Lot-level identifiers travel with each shipment so the receiving practice can log use at the patient record level for its own compliance records.
Account verification and medical director review
Every account requires a valid NPI number checked against the national registry, and we encourage the supervising physician or medical director to review product documentation before the practice's first order. We recommend confirming your practice's own policy on biologics purchasing with the North Carolina Medical Board and your legal counsel, since distributor registration does not replace a practice's internal regulatory review.
Setting up a new account
A practice manager can typically begin intake, and Precision Biologics supports the process with access to physician-level conversations about documentation, not clinical advice. Most Charlotte pain and physical medicine accounts move from initial inquiry to verified status once NPI confirmation and medical director sign-off are complete.
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
Does Precision Biologics work with physical medicine practices as well as pain management clinics?+
Yes. Accounts are open to licensed pain management and physical medicine practices, physicians, and other licensed clinics with a verifiable NPI number.
What should our medical director review before we open an account?+
We recommend reviewing the certificate of analysis, donor eligibility summary, and lot release record for the product lot in question, and confirming registration documentation independently rather than relying on marketing claims.
How quickly can a Charlotte practice receive a cryopreserved order?+
Cryopreserved lots ship overnight on dry ice in validated containers once an account is verified; your practice should have a staffed receiving window ready so the shipment can move directly into storage.