Our contract manufacturer tests every production run and issues Certificates of Analysis covering identity, potency, heavy metals, and microbials. Those documents live on this page so you can see the quality systems behind the supplements you take.
The documents below are representative of each formulation, not tied to the specific unit you received. Here's how to use them.
Scroll to the Manufacturer Testing Documentation section below. Each product has a published COA from the contract manufacturer covering identity, potency, and safety.
The full lab panel opens — ingredient identity, potency, heavy metals, microbials. Each with pass/fail flags against USP standards.
Lot-specific reports are not currently available. The documents below represent the full scope of third-party testing we can share. Questions? Email info@theelisemethod.com.
Representative Certificates of Analysis issued by our contract manufacturer, verified by ISO 17025-accredited laboratories. Tap a report to open the full PDF.
Important: These are manufacturer-issued Certificates of Analysis — representative of each formulation and its manufacturing processes. They are not tied to the specific batch or unit you receive, and they are issued in the manufacturer's name, not Vault IQ LLC DBA The Elise Method. Full disclosure below.
Max Detox
Lot AD251204
Oxy Burn
Lot OXY240301
Digestive Enzyme
Lot DEB251013
Issued in the manufacturer's name, not Vault IQ LLC DBA The Elise Method. Updated periodically · Last refreshed April 22, 2026.
The Certificates of Analysis (COAs) displayed on this page are provided by our contract manufacturer and reflect testing performed on production runs manufactured by that facility. These documents:
Lot-specific Certificates of Analysis are not currently available. The documents published above represent the full scope of third-party testing documentation we can share. Questions about the testing behind these formulas? Email info@theelisemethod.com and we'll share what we have from the manufacturer.
FDA Disclaimer: These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.
Standard panels used across manufacturer Certificates of Analysis. Panels vary by report — see each COA for the specific tests run on that production batch.
Confirms the ingredient in the capsule is exactly what the label says — verified by HPLC fingerprinting against certified reference material.
Measures the active compound per dose — confirming each capsule delivers the stated amount.
USP <233> screening for lead, arsenic, cadmium, and mercury — with limits well below FDA safety thresholds.
USP <2021> and <2022> testing for E. coli, salmonella, staph, yeast, and mold — every sample must pass.



Three supplements, taken in the same order every day. Start with one or get the bundle.
Questions about anything in the published testing documents? Email info@theelisemethod.com.
These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease.

FDA DISCLOSURE: The statements made regarding these products have not been evaluated by the Food and Drug Administration. The efficacy of these products has not been confirmed by FDA-approved research. These products are not intended to diagnose, treat, cure or prevent any disease. All information presented here is not meant as a substitute for or alternative to information from health care practitioners. Please consult your health care professional about potential interactions or other possible complications before using any product. The Federal Food, Drug, and Cosmetic Act require this notice.
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