Poppi 7OH Lab Tests & Batch Certificates of Analysis (COAs)

Every production lot of Poppi 7OH undergoes mandatory 6-panel analytical verification at an independent ISO/IEC 17025 accredited laboratory prior to packaging. Verify your blister pack batch code against our live Poppi 7OH lab tests registry below.

Our 6-Panel Analytical Testing Protocol

Poppi 7OH laboratory testing is designed to evaluate six key quality and safety benchmarks for finished tablet batches. These assessments focus on product potency, contaminants, chemical composition, and manufacturing consistency.

1. HPLC 7-OH Potency Assay: High-Performance Liquid Chromatography (HPLC) is used to measure 7-hydroxymitragynine content and assess whether the measured potency aligns with the product’s stated specifications.
2. Heavy Metals Testing (ICP-MS): Inductively Coupled Plasma Mass Spectrometry (ICP-MS) is used to screen for heavy metals, including arsenic, cadmium, lead, and mercury, to evaluate compliance with applicable quality standards.
3. Microbial and Mycotoxin Screening: Laboratory testing evaluates the presence of selected microorganisms, including Salmonella spp., Escherichia coli, and Staphylococcus aureus, as well as yeast, mold, and aflatoxins.
4. Residual Solvent Analysis (GC-MS): Gas Chromatography–Mass Spectrometry (GC-MS) can be used to detect and measure residual solvents that may remain from the manufacturing or extraction process.
5. Adulterant and Synthetic Compound Screening: Analytical screening evaluates product composition for unexpected substances, unlisted synthetic compounds, and potential adulterants.
6. Weight and Score Uniformity: Tablet weight and scoring are assessed to evaluate manufacturing consistency and the uniformity of tablet portions.

Quality and Transparency: Reliable laboratory documentation helps provide greater transparency into product composition and quality. Testing results should be supported by verified laboratory reports for the relevant production batch.