Vendor review in a multidisciplinary pain practice
Pain management and physiatry groups often split vendor evaluation between a medical director and a practice manager, with the medical director focused on documentation quality and the practice manager focused on ordering logistics and account setup. Common questions include whether a lot's sterility testing is complete before release from quarantine, whether a certificate of analysis is available for that specific lot, and whether a physician can speak with someone familiar with the documentation outside of a sales context.
Omaha
NPPES registry listings, primary taxonomy, retrieved 2026-10-27
116- Pain Medicine
- 40
- Physical Medicine & Rehabilitation
- 76
Confirming fit with Nebraska regulatory requirements
A practice's medical director and legal counsel are responsible for determining how a given product and its intended use fit the practice's regulatory posture, and should raise lot-specific or use-specific questions with the Nebraska medical board rather than with the distributor. Precision Biologics does not advise on dosing, procedures or indications, and provides screening and testing documentation to support the practice's own review.
NPI-verified ordering
Accounts are opened by submitting the practice's NPI number along with basic intake details, after which a representative verifies the account and releases access to product documentation and ordering. This process is identical for a solo physiatry practice and a larger multi-site pain management group.
- Practice or physician NPI number
- Practice contact and billing information
- Confirmation of licensure status
Delivery logistics for the Midwest
Cryopreserved Wharton's jelly ships overnight at -80 degrees Celsius on dry ice in validated containers, and a practice should have staff ready to receive and log the package the day it is scheduled to arrive. Lyophilized exosome formats are shelf-stable at room temperature per the insert included with the lot, which simplifies inventory handling for practices that stock multiple formats.
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
Do we need a physical office visit to set up an account?+
No. Accounts are verified remotely using the practice's NPI number and basic intake information.
Can a physical medicine practice and a pain management practice share one account?+
Each account is tied to a specific NPI, so practices operating under separate NPIs typically maintain separate accounts.
What happens if a shipment arrives without someone to receive it?+
Cryopreserved shipments are time-sensitive and should be received and logged on the scheduled delivery day; practices should coordinate staffing in advance for that reason.