Precision matters. And we prove it.
Every clinical product lot Radix supplies is tested by an independent third-party laboratory for potency, sterility, and endotoxin levels before it ships. We maintain compliance with USP <797> standards across all compounding partners, and Certificates of Analysis are available on request for any lot number. Our compounding partners are FDA-registered, state-licensed, and subject to regular audits.
What we test, and how.
Potency
Active ingredient quantification per lot to verify labeled strength.
Sterility
USP sterility testing performed before lot release.
Endotoxins
Bacterial endotoxin testing on every lot.
Facility audit
Regular audits and FDA-registration verification of compounding partners.
Need a Certificate of Analysis?
Email support@radixregenerative.com with your lot number and account name, or use the form below. COAs are returned within one business day.