Hemp Potency 12
Panel code HP-12Quantification of 12 cannabinoids commonly required for hemp products, reported as mg/g and % w/w for label claim support.
Tetex Lab provides testing and analytics for hemp & cannabis, nutraceuticals, cosmetics, and CPG products—delivering clear, interpretive COAs to support compliance and retail readiness.
Website information is a general overview of Tetex Lab services and does not replace formal quotes, contracts, or legal and regulatory advice. Testing availability may vary by jurisdiction.
Look up potency, safety, stability, and R&D panels by matrix, region, or regulatory focus. Final panel selection should match your jurisdiction.
A focused menu of methods supporting label claims, regulatory submissions, and R&D iterations for product teams.
Quantification of 12 cannabinoids commonly required for hemp products, reported as mg/g and % w/w for label claim support.
Cannabinoid potency plus a targeted terpene panel ideal for gummies, chocolates, and other infused edibles.
Potency plus microbiology, heavy metals, mycotoxins, residual solvents, and pesticides for regulated concentrate products.
Microbiological screening suitable for cosmetic and topical products, supporting quality and shelf-life programs.
Quantitative analysis of active ingredients in ready-to-drink beverages, supporting line trials and scale-ups.
Multi-time-point potency checks to support early stability observations on pilot or pre-launch batches.
From small-batch startups to multi-state operators, Tetex Lab helps teams align testing plans with compliance, retail, and investor expectations.
Standardized intake and reporting designed to keep documentation clean, reproducible, and audit-ready.
Align matrices and panels with your product roadmap and jurisdictional requirements, then lock in pricing.
Submit samples with digital chain-of-custody. Tetex Lab verifies intake and runs appropriate methods.
Access COAs in the portal, export reports for retailers, and collaborate on any next-round R&D or quality work.
Tetex Lab supports clients across multiple jurisdictions. Shipping, sample handling, and panel availability may vary by region and local rules.
Use this form to request pricing, turnaround estimates, and recommended panels for your product line or upcoming launch.
Use this channel for product complaints, suspected quality issues, or investigations that may require Tetex Lab involvement.
Product complaints may originate from consumers, retailers, or your internal QA team. Your own SOPs always control. This section illustrates a structured path for documenting issues and involving Tetex Lab where analytical work is needed.
This card outlines a dedicated Tetex complaint contact path. Configure this together with your QMS, ticketing, or other internal systems.
Educational content for product developers, QA teams, and compliance leads. These sample posts show how an insights section can be structured.
How product teams can align panel selection with label strategy, jurisdictional rules, and retailer expectations.
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A framework for timing full safety panels as you move from benchtop prototypes into commercial runs.
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How clear complaint documentation helps labs, regulators, and QA teams work together efficiently.
Read article →Before artwork is finalized, align on which actives will appear on the label, which cannabinoids or other ingredients matter in your market, and how often you plan to verify batches. A clear testing plan with Tetex Lab reduces relabeling and rework.
Early R&D panels focus on formulation and homogeneity. As you approach launch, coordinate with Tetex Lab on the compliance panel that matches your jurisdiction and retailer requirements, then standardize that panel for production runs.
Complaint files that capture lot, SKU, COAs, photographs, and communication history make it easier to assess risk, determine whether confirmatory testing is needed, and document decisions for regulators and partners.
Choose the option that best fits your question—commercial, technical, or general lab support.
Quotes for new projects, volume pricing, and multi-site programs.
Methods, reporting, and data interpretation for existing or planned panels.
Statements, account updates, and general administrative questions.