Food Contact
Compliance Support
End-to-end regulatory assistance for FDA, LFGB, EU 10/2011, and more. We help brands validate silicone products for food contact -- from material selection to third-party lab certification.
Target Market &
Product Use Confirmation
Every compliance journey starts with clarity. We work with you to map the exact regulatory landscape for your destination market and intended product application.
Market Mapping
US, EU, UK, Japan, Australia -- regulations differ. We identify which standards apply.
Use-Case Review
Baking, freezing, high-heat, baby products -- each triggers specific test protocols.
Risk Assessment
Pre-flag potential compliance risks before production begins.
Timeline Planning
Align testing cycles with your launch roadmap to avoid delays.
- Material Safety Data Sheet (MSDS) Ready
- Supplier Declaration of Compliance Ready
- Food-Grade Raw Material COA Ready
- Pigment & Additive Disclosure Ready
- Historical Test Reports Ready
Material Files &
Supplier Documentation
We maintain a comprehensive documentation library sourced directly from certified silicone material suppliers -- ready to submit alongside your test applications.
Every raw material batch is traceable, with MSDS, COA, and compliance declarations archived for audit readiness.
Sample, Color &
Test Scope Coordination
Testing isn't one-size-fits-all. We coordinate sample preparation, color variants, and precisely scoped test items to match your product's intended use.
Sample Preparation
Dedicated production runs for test samples, replicating final manufacturing conditions.
Color Variants
Each pigmented SKU is tested separately -- we prepare all color variants per spec.
Test Item Scoping
Migration, extraction, organoleptic -- we define the right test matrix for your market.
Third-Party Lab
Submission Support
We coordinate directly with globally accredited laboratories -- SGS, Intertek, TÜV, BV -- handling submission logistics, test specifications, and timeline management on your behalf.
Test Issue Analysis &
Material Adjustment
When a test flags an anomaly, our engineering team investigates the root cause -- adjusting formulation, pigments, or processing parameters until compliance is achieved.
Root Cause Diagnosis
Lab report deep-dive to isolate the failing substance or parameter -- migration, VOC, heavy metals, or odor.
Formulation Adjustment
Switch pigment grades, modify curing agents, or re-select base material to resolve non-compliance.
Re-Test & Validation
Submit revised samples for confirmation testing until the final report meets your target standard.
Batch Material &
Document Management
Compliance isn't a one-time event. We archive batch-level material records, test reports, and shipment documentation -- giving you traceability for every order, audit, and recall scenario.
| Batch | Material Lot | Report | Status |
|---|---|---|---|
| #B-2401 | SIL-A-0124 | LFGB-R-2401 | Archived |
| #B-2402 | SIL-A-0124 | FDA-R-2402 | Archived |
| #B-2403 | SIL-B-0224 | EU10/2011 | Archived |
| #B-2404 | SIL-B-0224 | LFGB-R-2404 | In Progress |
Need compliance for
your target market?
Share your product, destination market, and intended use. Our compliance team will reply within 24 hours with a tailored support plan.