Our pharma-grade FIBCs are made purely with brand new medical PP material, no recycled fabric used at all. The material itself is clean, odorless and free of any impurities. All production follows GMP guidelines, with every batch third-party tested. Heavy metal content, microorganism levels and residual dust all meet EU EP and US USP standards for pharmaceutical use. There is no chemical reaction with drug materials, so you don't have to worry about product contamination during storage and transit.
We use precision weaving for the outer fabric. The surface is smooth with no burrs, and it never sheds fibers - a key feature to avoid contaminating high-purity pharmaceutical materials. For internal protection, standard bags come with a sterile food-grade PE liner. We also offer aluminum foil sterile liners for higher hygiene demands.
All liners go through 121℃ high-temperature sterilization, reaching Class 100 cleanliness. We can upgrade to Class 10 ultra-clean standard upon request. To keep internal contents fully sealed, we combine sterile zip closure and heat sealing on the bag mouth. This tight seal keeps out dust, moisture and foreign impurities, maintaining a stable sterile environment for pharma materials from loading to final use.
Every stitch is done with dedicated sterile pharmaceutical polyester thread, free of fluorescent additives and strange odors. All materials are sterilized before sewing. We reinforce the bag bottom, corners and lifting strap joints with double stitching and backstitch work, plus sterile corner protectors. This prevents loose fibers, leakage and secondary contamination during handling.
We offer full custom support to fit different pharma working conditions. Bag dimensions can be adjusted freely for sterile warehouse storage, in-factory turnover and cross-border shipping. Stackable designs are available to help save warehouse space.
Material options are flexible too. Standard pharma-grade PP is for professional pharmaceutical packaging, while food-grade PP is available for cross-industry use. Liner thickness ranges from 0.13mm to 0.20mm, with PE and aluminum foil material options. We adjust sterilization methods including high-temperature and UV treatment, matching Class 10 or Class 100 cleanliness as required.
We can add double-layer sterile lining, fully sealed zip closure and leak-proof bottom structure for cleaner, residue-free unloading. Sterile corner protection parts are also optional to further reduce contamination risks.
Custom printing is supported with professional pharma-grade eco ink. You can print company logos, pharmaceutical warning marks, material info and sterility grades. The printing is clear, fade-proof and odorless, fully compliant with industry packaging norms.
We also do ODM custom development. Based on your material traits, cleanliness requirements and shipping methods, we adjust the whole packaging solution from design to sample confirmation. All processes follow GMP rules, providing one-stop packaging solutions and helping you avoid compliance issues.
FAQ
Q: Can you provide GMP and sterility test reports?
A: Yes, we have complete GMP, ISO 13485 and SGS sterility & cleanliness test documents. All certificates are verifiable. We accept third-party on-site inspections for sterility, cleanliness and heavy metal indicators, and fully cooperate with the whole testing process. Inspection fees can be negotiated to meet your industry standards.
Q: How do you handle packaging and logistics?
A: Finished bags are packed with sterile film and placed on pre-sterilized pallets to avoid transit contamination. We support sea, air and land shipping, covering over 50 global ports, and can deliver to your designated sterile warehouse or factory. For sea freight, we use double-layer sterile wrapping for better moisture and pollution resistance. We have plenty of successful aseptic shipping cases with complete traceable records.
Q: What if custom sterility and cleanliness do not meet my standard?
A: We provide full test certificates with pre-production samples. If you are not satisfied with the sample performance, we will adjust the solution, remake samples and redo sterilization and testing for free. We only start mass production after your final confirmation, with no extra sampling or testing charges.
Q: How do you solve sterility or cleanliness quality problems after delivery?
A: If you receive goods with non-human-caused issues like fiber shedding, dust residue or unqualified sterility, you can send photos, videos and test proofs to us. We will confirm the problem quickly and arrange free replacement or full refund, covering all logistics costs. Supplementary test reports will be provided in time to ensure your production is not affected and avoid compliance risks.
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