The GLP-1 Off-Ramp: Opportunity for Supplement Founders
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Every production run ships with a COA from an ISO 17025 accredited lab. We don't cut corners here. It protects your brand and your customers.
Quality testing isn't an add-on. It's built into every production run. Every batch ships with a Certificate of Analysis (COA) from an ISO 17025 accredited third-party laboratory. No exceptions.
Standard testing covers identity verification (confirming you got what you paid for), potency testing (confirming the label matches reality), heavy metals screening (lead, mercury, arsenic, cadmium), and microbial contamination checks. Depending on your product and regulatory requirements, we may add pesticide residue testing, allergen screening, or stability studies.
This isn't just about compliance. It's about protecting your brand. One contaminated batch can end a supplement company. We've seen it happen. Our testing protocols are designed to catch problems before they reach your customer.
Certificate of Analysis (COA) included with every batch
Heavy metals, microbial, and pesticide screening standard
Potency verification to confirm label accuracy
Every COA comes from an accredited third-party lab. Not an in-house test, not a self-certification. Independent, verifiable results.
Identity, potency, heavy metals, microbial, and pesticide testing as standard. Additional panels available based on your product profile.
COAs give retailers and consumers confidence in your product. Many Amazon and retail buyers now require them before placing orders.
Our GMP-certified partner facilities run in six regions across Canada and the United States. Each region page covers the local network, dosage forms, and regulatory ground.
Tell us about your project and we'll put together a plan and quote tailored to your product, timeline, and budget.