| Product specification | Confirm bag style, dimensions, thickness or fabric construction, weight capacity, closure, printing, and intended use. | A controlled specification drawing or datasheet that identifies tolerances and the agreed inspection method. | Approve a production sample against written requirements; do not rely on a quotation description alone. |
| Material identification | Determine whether the bag is made from woven polypropylene, polypropylene film, or a stated combination of materials. Clarify coatings, liners, inks, and additives. | Material declaration, bill of materials, and lot-linked certificates or test reports where material identity is critical. | Require written approval before any material, additive, coating, or manufacturing-process substitution. |
| Mechanical performance | Evaluate strength and durability using tests suited to the bag construction and use, such as tensile, tear, seam, drop, or filled-bag tests. | Test reports stating the sample, conditioning, method, results, and acceptance limits. ASTM D882 can be relevant to tensile properties of thin plastic sheeting; ASTM D1709 and ASTM D1922 address specific impact and tear tests, respectively, when applicable. | Set pass/fail limits for the actual bag and application. Test methods describe how to test; they do not, by themselves, establish a universal product limit. |
| Quality management | Review controls for incoming materials, production checks, nonconforming products, corrective actions, and change management. | Current ISO 9001 certificate, if claimed, with its scope and issuing certification body; request audit or quality-control records relevant to the product. | Confirm certificate validity and scope independently. ISO 9001 certification concerns a quality management system, not automatic certification of every bag. |
| Food-contact suitability | If the bag will contact food, verify the rules for the destination market, food type, contact time, temperature, and intended conditions of use. | A material-specific compliance declaration and supporting migration or other test reports appropriate to the intended use. For the EU, assess applicable requirements including Regulation (EU) No 10/2011 for plastic food-contact materials; in the United States, assess applicable FDA requirements, including relevant provisions of 21 CFR 177.1520 where appropriate. | Accept documentation only when it covers the actual formulation, bag construction, use conditions, and destination market. A generic “food grade” statement is not sufficient evidence by itself. |
| Chemical and market compliance | Identify applicable chemical, packaging, labeling, and restricted-substance rules based on product use and sales destination. | A dated regulatory declaration that names the market and applicable requirements, supported by relevant test results or material disclosures where needed. | Check each market separately. Requirements such as REACH obligations depend on the substance, article, and supply-chain circumstances; do not treat a broad compliance claim as proof for every regulation. |
| Recycled content claims | If recycled polypropylene is specified, clarify the claimed percentage, whether it is post-consumer or post-industrial material, and any performance or use restrictions. | A documented calculation and traceability records linking the claim to material inputs and production lots; request independent verification if required by the buyer or market. | Make claims precise and supportable. Confirm that recycled content is suitable for the intended application and any applicable food-contact rules. |
| Traceability and records | Check whether finished bags can be linked to production dates, material lots, specifications, and inspection results. | Sample batch records, lot codes, certificates of analysis where relevant, and a documented record-retention process. | Agree how quickly the supplier can trace an affected lot and provide supporting records if a quality or compliance issue occurs. |
| Sampling and inspection | Agree inspection points for dimensions, appearance, printing, seams, quantity, and functional performance. | A written inspection plan and sample reports. If using ISO 2859-1, specify the sampling plan and acceptance criteria in the purchase agreement. | Define acceptance limits before production. Sampling plans support inspection decisions but do not replace clear product specifications. |
| Change control and supply continuity | Assess how changes to raw materials, tooling, production locations, or subcontractors are communicated and approved. | Written change-notification procedure, lead-time information, and a documented escalation contact for quality or compliance issues. | Require advance notice and re-approval when a change could affect fit, performance, traceability, or regulatory status. |