USP 795/797/800 Compliant|Licensed 503A Pharmacy|COA on Every Batch|Same-Day Compounding|Free Shipping on Qualifying Orders
Quality & Compliance

Uncompromising Quality. Total Transparency.

Every compound we produce is dual-tested: in-house QC plus independent third-party verification. Every result is published. No exceptions.

Our Protocol

Dual-Layer Quality Testing

While most pharmacies rely on a single round of testing, we verify every batch twice — first in-house, then through an independent accredited laboratory.

Layer 1: In-House QC

Every compound, every time

  • Visual inspection and organoleptic testing
  • Weight/volume verification against formula
  • pH testing for all liquid preparations
  • Initial potency check via UV spectrophotometry
  • Beyond-use dating verification
  • Labeling accuracy review

Layer 2: Third-Party Verification

Independent accredited lab

  • HPLC purity and potency analysis
  • Mass spectrometry identity confirmation
  • Sterility testing (USP <71>) for sterile preps
  • Bacterial endotoxin testing (LAL method)
  • Particulate matter testing (USP <788>)
  • Full Certificate of Analysis generation
Compliance

USP Standards Compliance

USP 795

Non-Sterile Compounding

Governs personnel training, facility requirements, quality assurance, and documentation for non-sterile compounded preparations.

  • Personnel qualifications
  • Component selection
  • Stability criteria
  • Quality assurance program
USP 797

Sterile Compounding

Establishes standards for compounding sterile preparations including environmental controls, personnel training, and quality testing.

  • ISO Class 5/7/8 cleanrooms
  • Environmental monitoring
  • Media fill testing
  • Sterility & endotoxin testing
USP 800

Hazardous Drug Handling

Sets requirements for safe handling of hazardous drugs throughout the compounding process, from receipt to disposal.

  • Containment engineering controls
  • Personal protective equipment
  • Decontamination protocols
  • Waste management
COA Library

Certificate of Analysis Records

Search by product name or batch number to find testing results.

ProductBatch #Test DatePurityStatus
Semaglutide Injection 2.5mg/mLNVX-SEM-2025-08472025-12-0199.2%Pass
Tirzepatide Injection 5mg/mLNVX-TRZ-2025-09122025-11-2898.8%Pass
Testosterone Cypionate 200mg/mLNVX-TES-2025-06332025-11-1599.5%Pass
Progesterone Capsules 200mgNVX-PRG-2025-07212025-11-1099.1%Pass
Semaglutide Injection 5mg/mLNVX-SEM-2025-08482025-12-0399.4%Pass
Estradiol Cream 0.5mg/gNVX-EST-2025-04552025-10-2298.9%Pass
Ketamine Nasal Spray 50mg/mLNVX-KET-2025-03012025-10-1599.3%Pass
Tretinoin Cream 0.05%NVX-TRT-2025-01892025-10-0899.0%Pass

Quality You Can Verify

Have questions about our testing protocols, facility credentials, or a specific COA? Our quality team is always available.

Contact Quality Team