Verification Audit Trail

Pharmacy Network Verification

12 vetted 503A and 503B compounding partners behind every Veridian shipment. Every listing on this page has passed the same multi-step verification methodology below — and we re-verify annually.

Our verification methodology

Every pharmacy in the Veridian network passes a five-step review before listing. We re-run verification on an annual cadence and monitor regulatory alerts in real time. The framework below exists because post-FDA enforcement on semaglutide compounding has materially tightened the line between compliant 503A patient-specific dispensing and 503B office-use outsourcing — and clinics deserve to see how that line is enforced on their behalf.

  • State licensure across all 50 states. Every license is checked against the relevant state board of pharmacy database before listing.
  • PCAB or ACHC accreditation on file. Pharmacy Compounding Accreditation Board or Accreditation Commission for Health Care documentation is reviewed and verified directly with the accreditor where possible.
  • FDA registration status for 503B partners. Outsourcing facility registration is checked on the FDA public registry, including current cGMP compliance posture.
  • Clean 483-observation history. No unresolved Form 483 observations in the prior 24 months, and no open warning letters for compounding deficiencies.
  • Certificate of Analysis for every compound. Each in-network compound has a per-batch CoA on file covering potency, sterility, and endotoxin where applicable.
On NPI verification: Provider-side NPI verification is enforced separately as part of clinic onboarding. The verification data on this page covers pharmacy-level licensure, audit history, and compounding scope — not the prescribing credentials of your own clinic.
503A Patient-Specific Compounding Pharmacies

503A Patient-Specific Compounding Pharmacies

State-board-licensed pharmacies compounding patient-specific prescriptions under USP standards. Each order requires a valid prescription for an identified patient.

503B FDA-Registered Outsourcing Facilities

503B FDA-Registered Outsourcing Facilities

FDA-registered outsourcing facilities operating under cGMP, producing office-use batches for physician dispensing across state lines.

Ready to source through a verified network?

Apply with your NPI and we'll match you to the partners cleared for your patient population. Onboarding typically completes in 3–5 business days.

Apply for provider access →