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A
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AAFCO (Association of American Feed Control Officials)
Certifications
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AAFCO is the standard-setting body for pet food and animal feed in the U.S. Sets ingredient definitions, labeling rules, and nutritional adequacy criteria — adopted into law by most states.
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B
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Batch Testing
Process
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Batch testing is per-lot release testing that confirms each production run meets specification before it ships. Without batch testing, you have no recall traceability.
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C
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cGMP (Current Good Manufacturing Practices)
Certifications
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cGMP (current Good Manufacturing Practices) is the FDA's modernized version of GMP — same framework, but the 'current' part requires manufacturers to update methods and equipment as technology advances.
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Co-Manufacturing / Co-Packing
Sourcing Models
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Co-manufacturing (co-man) is contract production of finished goods. Co-packing (co-packer) is contract packaging of bulk product into retail format. Both are dominant terms in food and beverage CPG.
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COA (Certificate of Analysis)
Process
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A Certificate of Analysis (COA) is a per-batch quality document that certifies a finished product or raw material meets its written specifications.
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COGS (Cost of Goods Sold)
Volume & Cost
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COGS (Cost of Goods Sold) is the per-unit production and acquisition cost of inventory. Manufacturing + packaging + inbound freight + duties. Nothing else.
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Contract Manufacturing
Sourcing Models
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Contract manufacturing is dedicated production at a third-party facility, built to your custom spec. Your formula, your IP, their line.
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Custom Mold Tooling
Packaging
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Custom mold tooling is the dedicated equipment built to produce a unique packaging component. High upfront cost, high lead time, full proprietary design control.
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D
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Drop Shipping (vs Private Label)
Sourcing Models
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Drop shipping is a fulfillment arrangement where the supplier ships directly to your customer. It is an operations model, not a branding model — you can drop-ship generic or private-label goods.
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DSHEA (Dietary Supplement Health and Education Act)
Certifications
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DSHEA is the 1994 federal law that defines dietary supplements as a food category in the U.S. Establishes labeling, claims, and ingredient rules — and the difference between supplements and drugs.
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E
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EAU (Estimated Annual Usage)
Volume & Cost
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EAU (Estimated Annual Usage) is your honest twelve-month volume forecast for a SKU, given to the manufacturer for pricing-tier setup.
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F
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FDA Registration vs FDA Approval
Certifications
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FDA registration is a public listing of facilities. FDA approval is a regulatory clearance of a specific product. A 'FDA-registered facility' does not mean a 'FDA-approved product' — the two are entirely different.
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Formulation
Process
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Formulation is the process of converting a product concept into a stable, scalable, manufacturable specification. The deliverable is a master formula document.
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G
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GMP (Good Manufacturing Practices)
Certifications
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GMP (Good Manufacturing Practices) is the baseline regulatory framework for how a manufacturer must operate to produce safe, consistent products. Required by FDA for supplements, drugs, and many food categories.
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Gross Margin
Volume & Cost
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Gross margin is (Revenue - COGS) / Revenue, expressed as a percentage. It measures how much each dollar of sales contributes after direct production cost.
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I
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ISO 22716 (Cosmetics GMP)
Certifications
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ISO 22716 is the global GMP standard for cosmetics manufacturing. EU-required, U.S.-recommended, and increasingly enforced under MoCRA.
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K
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Kosher / Halal
Certifications
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Kosher and Halal are independent religious certifications administered by accredited agencies that audit ingredients, equipment, and production for compliance with Jewish (kashrut) or Islamic (halal) dietary law.
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L
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Landed Cost
Volume & Cost
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Landed cost is the all-in per-unit cost of getting inventory from the factory dock to your warehouse: factory price + freight + duties + brokerage + insurance.
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Lead Time
Process
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Lead time is the elapsed time from purchase order signed to finished goods delivered to your warehouse. Includes raw materials, production, QC, packaging, and shipping.
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M
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MoCRA (Modernization of Cosmetics Regulation Act)
Certifications
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MoCRA is the 2022 federal law that modernized U.S. cosmetics regulation. New requirements: facility registration, product listing, safety substantiation, adverse event reporting, GMP.
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MOQ (Minimum Order Quantity)
Volume & Cost
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MOQ (Minimum Order Quantity) is the smallest production run a factory will accept for a given SKU. It is set by the factory's cost recovery math, not by your marketing math.
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N
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NSF Certification
Certifications
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NSF certification is third-party verification that a product or facility meets specific safety, quality, or content standards. Different NSF certifications cover different things — pick the one that fits your claim.
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O
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ODM (Original Design Manufacturer)
Sourcing Models
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An ODM (Original Design Manufacturer) develops the product design and formula in-house, then licenses it to multiple brands who sell it under their own labels.
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OEM (Original Equipment Manufacturer)
Sourcing Models
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An OEM (Original Equipment Manufacturer) is a factory that builds products to your spec, under your brand. You bring the design or formula; they bring the production line.
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P
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Primary Packaging
Packaging
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Primary packaging is the container that directly holds and protects the product. Drives shelf life, perceived quality, and unit cost.
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Private Label
Sourcing Models
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Private label manufacturing is when a contract factory produces a product packaged exclusively under your brand. You own the brand; the factory owns the formula and the production line.
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S
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Sample Run / Pilot Run
Process
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A sample run is a marketing-quality small batch (50-500 units). A pilot run is a production-process validation batch (5-10% of full run scale). They serve different purposes — do both for custom SKUs.
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Secondary Packaging
Packaging
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Secondary packaging is the outer carton, sleeve, label, or insert wrapping the primary container. The main canvas for branding and the primary retail-shelf surface.
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Stability Testing
Process
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Stability testing is the structured evaluation of how a product's quality changes over time under defined storage conditions. Establishes shelf life and validates packaging.
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Stock Packaging
Packaging
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Stock packaging is off-the-shelf bottles, jars, and cartons held in inventory by the manufacturer. No tooling cost, fast lead time, predictable unit cost.
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T
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Third-Party Testing
Process
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Third-party testing is independent lab verification of label claims and product safety, performed by an organization with no financial interest in the result.
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Tooling Costs
Volume & Cost
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Tooling costs are one-time charges for the custom production equipment (molds, dies, plates) needed to make a unique packaging or product format.
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U
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USDA Organic
Certifications
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USDA Organic is a federal certification with four labeling tiers based on the percentage of organic ingredients. Only certified facilities producing certified products can use the USDA Organic seal.
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W
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White Label
Sourcing Models
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White label is a pre-made stock product that a manufacturer sells to multiple retailers under each retailer's own brand. Same formula, same packaging spec, different logos.
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