What documentation to request before approving a new supplier
Pain management and physical medicine groups that bring in a new tissue or biologics supplier typically start by requesting the same records a hospital-affiliated purchasing committee would ask for: a certificate of analysis, a donor eligibility summary, and a description of how the lot was tested before release.
Because Pain Medicine and Physical Medicine & Rehabilitation providers in Reno span both solo practices and larger multidisciplinary groups, the level of internal review can vary; Precision Biologics provides the same lot-level records to every verified account regardless of practice size.
- Certificate of analysis by lot
- Donor eligibility and serology screening summary
- Processing and recovery timeline description
- Sterility testing and lot release confirmation
Reno
NPPES registry listings, primary taxonomy, retrieved 2026-10-27
89- Pain Medicine
- 35
- Physical Medicine & Rehabilitation
- 54
Regulatory review stays with your practice
Precision Biologics distributes Wharton's jelly products under the supplier's HCT/P framework and exosome products as biologic articles that are not FDA approved; neither classification is a clinical recommendation, and whether a specific intended use is appropriate is a determination for your physician and counsel.
Reno practices should confirm their own scope-of-practice and supervision requirements with the Nevada State Board of Medical Examiners, the Nevada State Board of Osteopathic Medicine, or applicable nursing board, depending on who is ordering on the account.
Shipping and receiving in northern Nevada
Cryopreserved products are held at -80 degrees C and ship overnight on dry ice in validated containers; lyophilized formats ship at ambient temperature and are described by the supplier as shelf-stable. Front-desk or clinical staff receiving a shipment should confirm the container integrity and log the lot number immediately.
Traceability is maintained by recording the lot number against the patient record at the point of use, which matters for any future documentation request.
Setting up a verified account
Accounts require a valid NPI number tied to a licensed physician. Once verified, your practice can request documentation by lot and arrange a peer-to-peer call between your physician and a Precision Biologics contact to review available records in more detail.
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 multidisciplinary pain practice in Reno order more than one product family?+
Yes. A single verified account can order both Wharton's jelly and exosome product families; documentation is provided separately for each because they carry different regulatory classifications.
Who at our Reno practice needs to be listed on the account?+
The account is tied to a licensed physician's NPI number. Additional ordering staff can be added once that physician's verification is complete.
Does Precision Biologics recommend which product to use for a specific case?+
No. Precision Biologics provides sourcing, testing and documentation support only; decisions about clinical use belong to your physician and your practice's own protocols.