For Compounding Pharmacies

API-Grade Peptides for
Compounding Excellence

Clariven Labs provides compounding pharmacies with pharmaceutical-grade Active Pharmaceutical Ingredients (APIs) backed by complete regulatory documentation and batch traceability.

Built for Pharmacy

Your Compounding Partner, Not Just a Supplier

We understand the unique regulatory, quality, and operational demands of compounding pharmacies — because we built our supply chain around them.

503A/503B Compliance

Complete documentation packages designed for both patient-specific (503A) and outsourcing facility (503B) requirements under federal and state regulations.

Full COA & Documentation

Batch-specific COAs with HPLC, MS, endotoxin, sterility results plus safety data sheets, stability reports, and supplier qualification files.

Bulk API Supply

Gram-to-kilogram quantities with consistent lot sizes. Multi-lot reservations available for high-volume compounding operations.

GMP-Grade Packaging

Properly labeled, sealed, and stored APIs arrive in pharmaceutical-grade packaging with tamper-evident seals and temperature indicators.

Reliable Supply Chain

Multi-source manufacturing network eliminates single-point-of-failure risks. Safety stock programs available for critical formulations.

Facility Audit Support

We support your Board of Pharmacy inspections with supplier qualification documentation, audit histories, and regulatory correspondence.

Regulatory Ready

Compliance Documentation That Passes Inspection

State board inspections and FDA audits require meticulous documentation of your API supply chain. Clariven Labs provides the complete documentation package your pharmacy needs to demonstrate compliance.

Batch-specific Certificates of Analysis (COAs)
Certificate of Conformance for each lot
Supplier qualification and audit reports
Safety Data Sheets (SDS) for all products
ICH-compliant stability study data
cGMP manufacturing facility documentation
Chain of custody and traceability records
Drug Master File (DMF) reference letters

Quality by the Numbers

≥98%

Minimum Purity

100%

COA Coverage

<0.5

EU/mg Endotoxin

USP

Testing Standards

6-Point

Analytical Panel

ICH

Stability Protocol

“As a 503B outsourcing facility, supplier qualification is critical. Clariven Labs provides the most complete documentation package we've seen from any peptide API supplier.”

Michael Torres, RPh

Director of Quality, Regional Compounding Pharmacy

Upgrade Your API Supply Chain

Request bulk pricing, sample COAs, or schedule a call with our pharmacy sales team. We'll show you why leading compounders choose Clariven.