Manufacturing insights
What we've learned building supplements for brands worldwide — cGMP, formulation, formats, and where the industry is going.
Quality & ComplianceNew Dietary Ingredient (NDI) Notification
An ingredient first marketed after 1994 is a New Dietary Ingredient. Using one without an NDI notification can pull your product off the shelf.
ManufacturingPrivate Label Supplement Launch Timeline
From first call to first shipment, a realistic timeline for a private label supplement launch and where you can compress the stages.
Quality & ComplianceSupplement Registration vs Notification
In the U.S. you don’t register a supplement — you notify. The distinction sounds pedantic until it delays your launch. Here’s how it works.
Getting StartedHow to Brief a Contract Manufacturer
The difference between a vague inquiry and a 24-hour actionable quote is a clear brief. Here is the checklist we ask every brand to complete.
FormulationSoftgels vs Capsules: Which Format?
Softgels and two-piece capsules are made differently, suit different actives, and carry different costs. A side-by-side comparison.
ManufacturingSoftgel Stability Mistakes That Kill Launches
Oxidation, leaking shells, and bloom are not bad luck — they are briefing and process failures. How to brief softgel projects so they survive.
Getting StartedOEM vs ODM vs Private Label
Three routes to a supplement on the shelf, each with a different split of work, cost, and ownership. A practical guide to picking the right one.
Quality & ComplianceBuilding a Retail-Ready Spec Sheet
Retail and marketplace onboarding fail when the spec sheet is marketing copy. Here is the manufacturing-grade checklist that keeps production aligned.
Getting StartedWhat Is MOQ in Supplement Manufacturing?
MOQ is the single number that shapes your launch cost and timeline. Here’s what it means, why manufacturers set one, and how to use it.







