At VitaEver Nutrition, purity isn’t just a claim — it’s a documented commitment to U.S. regulatory standards. Every supplement batch is tested under ISO 17025–accredited laboratory protocols in Sacramento, CA, ensuring compliance with FDA and cGMP requirements.

  • Heavy Metal Screening (ICP-MS): Raw materials are randomly sampled and analyzed using Inductively Coupled Plasma Mass Spectrometry to detect lead, mercury, arsenic, and cadmium. All results must fall below 0.1 ppm, meeting strict U.S. safety thresholds.
  • Potency Verification (HPLC): Each serving is confirmed via High-Performance Liquid Chromatography to contain at least 99.8% active ingredient, guaranteeing label accuracy and eliminating unnecessary fillers.
  • Microbiological Safety: Independent third-party audits verify microbial counts under 10 CFU/g, well beneath USP and FDA limits, ensuring products are free from harmful pathogens.

Transparency You Can Trust

Every VitaEver bottle features a QR code linking directly to the Certificate of Analysis (COA) for that specific batch. Customers can instantly review lab results, ingredient sourcing, and final QC sign-off—providing full traceability and compliance with FTC advertising transparency guidelines.

Our Commitment

From sourcing to final packaging, VitaEver follows FDA Good Manufacturing Practices (cGMP) and exceeds industry standards. This multi-step protocol ensures you’re fueling your body with supplements that are:

  • Scientifically validated
  • Legally compliant with U.S. regulations
  • Safe, potent, and transparent

That’s Lab-Tested Purity by VitaEver Nutrition — backed by science, verified by independent labs, and aligned with U.S. regulatory requirements.