Identity & potency
HPLC confirms each active is present and matches the label dose.
Quality & testing
How Nervory is tested for quality
Nervory is made in an FDA-registered, cGMP-certified facility in the United States, and every production batch is screened by an independent laboratory before it ships. This page explains the process; the verification page shows the result for the current batch.
Manufacturing standards
Nervory is produced under current Good Manufacturing Practices (cGMP) in an FDA-registered facility. That covers documented procedures, qualified equipment, sanitation controls, and batch records for traceability. cGMP is about how the product is made consistently and cleanly; the lab testing below confirms what is actually in each batch.
What the third-party lab checks
Heavy metals
ICP-MS screening for lead, arsenic, cadmium, and mercury against strict limits.
Microbial limits
Testing for total counts and pathogens within USP limits.
Allergens & purity
Non-GMO inputs with checks for common allergen cross-contact.
Independent laboratory
Batch screening is performed by Northgate Chromatics Labs, LLC, an ISO/IEC 17025 accredited third-party laboratory. Using an outside lab means the results are not graded by us. The certificate of analysis for the current batch (NVY-26C2-0481, certificate NGC-2026-0774-V) reports 99.2% active purity by UHPLC-PDA, heavy metals under 0.6 ppm, and a pass on microbial screening.
Allergens and suitability
Nervory capsules are vegetarian (HPMC) and made without added gluten, dairy, or soy. As with any supplement, if you have allergies, a medical condition, or take medication, review the full ingredient list on the ingredients page and check with your physician first.
Testing details are provided for product authenticity and quality presentation and are not external clinical certifications of health outcomes.
Last updated: June 2026