HiSiaddi is an innovative foreign trade service provider driven by dual engines of technology transformation and foreign trade services, with a "1+2+3+4=1" service system and supply channels for original factory compound NSP enzymes from multiple well-known brands. Boasting over a decade of market experience and technological transformation cooperation with manufacturers, HiSiaddi possesses extensive expertise in product compliance issues. Below is a case of HiSiaddi resolving compliance problems for compound non-starch polysaccharide enzymes.
Please contact HiSiaddi customer service for further inquiries regarding compound NSP enzyme compliance issues.
The cooperating client is InVivo from France, a top-tier European agricultural and animal husbandry cooperative group specializing in high-end organic livestock and poultry feed, breeder premixes and pet food additives, operating across core EU markets including France, Germany and Belgium and supplying EU-certified organic pastures, precision breeding bases and premium pet brands. The company strictly complies with EU Feed Additive Regulation (EC) No 1831/2003, FAMI-QS, EFSA, non-GMO and full-traceability standards, with a compliance team consisting of EU registered compliance officers, food safety specialists and customs declaration professionals. Its requirements for imported feed additive authorization qualifications, document completeness, labeling standardization, strain safety and batch traceability meet official EU audit standards.
In January 2026, the client planned procurement of Chinese compound NSP enzymes for organic broiler/laying hen diets. Three domestic manufacturers contacted initially failed to satisfy full EU compliance requirements: lack of EU authorization qualifications, incomplete/non-standard documents, labels violating CLP regulations, unidentified strain sources and absent traceability systems. Two sample shipments were detained by French customs, risking return shipments, project delays and supply chain disruption. The client urgently commissioned HiSiaddi to complete compliance diagnosis, qualification supplementation, document restructuring, label rectification, traceability system construction and customs clearance support within 15 days; otherwise, all China procurement would be abandoned in favor of local European suppliers from Denmark and the Netherlands.
Core EU Regulation (EC) No 1831/2003 stipulates all feed additives (including enzymes) must be listed on the EU authorized list, complete EFSA safety assessments and hold EU Commission authorization numbers to qualify for import and sale.
Client pain point: All contacted domestic manufacturers lacked EU authorization qualifications; unlisted additives are classified as prohibited imports by French customs.
Underlying risks: Low-end clients may clear goods via informal channels, yet mid-to-high-end groups like InVivo prohibit non-compliant operations, which carry heavy fines, placement on EU industry blacklists and permanent market bans.
The client requires a full set of official English documents, yet domestic manufacturers universally suffer four document flaws: missing files, incorrect content, disordered formatting and no English translations.
1. Mandatory documents missing: English COAs, non-GMO declarations, FAMI-QS certificates, strain safety reports, heavy metal/microorganism test reports and certificates of origin.
2. Non-standard document content: Testing based on Chinese GB standards without EU EN/ISO reference data; enzyme activity units inconsistent with EU standards (U/g unaligned with corresponding EC numbers).
3. Language & formatting errors: Full Chinese documents without English translations; lack of official headers, signed seals and batch linkage eliminating traceability. Direct consequence: French customs and EFSA reject submissions with incomplete document packages, detaining samples at ports.
EU CLP Regulation (EC) No 1272/2008 mandates all labels be in English with complete information including product name, enzyme composition & EC numbers, production strains, batch numbers, shelf life, net weight, manufacturer details, EU Responsible Person (EC Rep), safety warnings and storage conditions.
Client pain point: Full Chinese labels without English translations; missing EC numbers, strain origins and EU Responsible Person information; absent allergen safety warnings; no batch traceable QR codes.
Risks: In addition to customs clearance barriers, non-compliant labeling prevents entry into EU supermarkets and high-end pastures due to mandatory full-chain traceability rules for mid-to-high-end products.
EU organic and safety requirements mandate NSP enzyme production strains be non-GMO QPS (Qualified Presumption of Safety) strains with supporting strain identification reports, genetic stability reports, non-GMO test certificates and non-pathogenicity verification.
Client pain point: Domestic manufacturers cannot provide detailed strain data beyond generic labels of "fungal/bacterial fermentation"; absent QPS safety certifications, genetic stability data and GMO testing reports; partial genetically modified strains disqualify products for organic feed applications. Direct impact: The client cannot obtain organic feed certification, and end pastures reject product usage, rendering procurement meaningless.
HiSiaddi assembled a dedicated team of EU compliance officers, FAMI-QS auditors, enzyme technical specialists, English document specialists and customs clearance consultants, cooperating with two domestic specialized enzyme manufacturers holding full EU export qualifications. We adopted a six-step workflow: compliance diagnosis → qualification matching → document restructuring → label rectification → traceability system construction → customs clearance support, fully aligned with EU standards with full English documentation, traceable data and one-pass audit approval. The client’s compliance team participated throughout with real-time audit progress updates.
1. Qualification diagnosis: Verification confirmed all contacted domestic manufacturers lacked Regulation (EC) No 1831/2003 authorization numbers, requiring screening of manufacturers with existing EU authorization or rapid supplementary qualification capacity.
2. Document diagnosis: Cross-check against the EU 21 mandatory document checklist identified 12 missing files and 5 non-standard documents without English versions.
3. Label diagnosis: CLP regulation audit revealed 8 critical missing data points, full Chinese text and absent traceable QR codes.
4. Strain diagnosis: Review of strain materials confirmed missing QPS certifications, GMO test reports and genetic stability data, with partial genetically modified strains incompatible with organic standards.
Based on diagnostic results, HiSiaddi screened two domestic mid-to-high-end enzyme manufacturers with valid EU FAMI-QS certification, non-GMO QPS strains and capacity to supplement full authorization documents:
1. Manufacturer X (Wuhan Xinhuyang): Xylanase/β-glucanase produced via non-GMO QPS strains Bacillus licheniformis and Trichoderma reesei, holding FAMI-QS, ISO 22000 and non-GMO certifications, capable of supplying strain identification, genetic stability and safety assessment reports.
2. Manufacturer Y (Guangdong Yiduoli): Products listed on the EU feed additive filing register with EU Responsible Person authorization letters, certificates of origin and EU-standard test reports, with extensive supply track record for high-end EU clients.
Core actions: Assisted the client in signing supplementary compliance agreements with both manufacturers, clarifying full liability for qualification guarantees, document provision, label rectification and traceability to ensure 100% compliance with zero subsequent risks.
Aligned with dual standards of EU EFSA and French customs, HiSiaddi restructured 21 official English documents with line-by-line audit, signed seals and batch linkage to guarantee one-pass audit approval.
1. English COA: Enzyme activity labeled with EC numbers + U/g (e.g. Xylanase EC 3.2.1.8, 12,000 U/g), testing conducted per EN/ISO standards with batch, shelf life and test date information.
2. Dual-stamped non-GMO declaration by manufacturer and HiSiaddi confirming non-GMO production strains, raw materials and carriers, attached with third-party GMO test reports.
3. Valid English FAMI-QS certificates covering full production workflows.
4. Strain safety reports: QPS certification, strain identification, genetic stability and non-pathogenicity verification issued by EU-accredited laboratories (English version).
5. Heavy metal/microorganism test reports (EU EN standards): Pb <5ppm, As <2ppm, Cd <1ppm, negative for Salmonella and E. coli.
6. Customs-issued English certificates of origin with full traceability.
7. EU Responsible Person (EC Rep) authorization letter with full French local compliance institution address, contact details and valid authorization term.
8. Batch traceability reports: Full-chain traceability covering raw material batches → production batches → finished product batches → test batches → delivery batches, paired with QR codes.
9. Safety Data Sheets (SDS) complying with CLP regulations, detailing allergen risks, storage conditions and emergency response protocols.
10. Supplementary supporting documents: ISO 22000, HACCP, organic feed compatibility certificates and packaging material safety reports.
HiSiaddi redesigned English labels and traceable packaging to meet dual requirements of EU CLP and client organic certification standards:
· Product Name: Compound NSP Enzyme (for Organic Poultry Feed)
· Enzyme Composition: Xylanase (EC 3.2.1.8) 12,000 U/g, β-Glucanase (EC 3.2.1.6) 2,500 U/g, Mannanase 3,000 U/g, Pectinase 2,000 U/g, Cellulase 500 U/g
· Production Strains: Bacillus licheniformis / Trichoderma reesei (Non-GMO, QPS)
· Core Information: Batch No., Expiry Date, Net Weight, Full Manufacturer Name/Address/Contact, Full EC Rep French Address/Contact
· Safety Warning: Contains enzyme protein, may cause sensitization
· Traceable QR Code: One-click access to full batch traceability reports, test reports and compliance documents
25kg food-grade kraft paper bags with PE inner liners for moisture and contamination resistance; outer cartons affixed with English labels, traceable QR codes and EU identification marks.
Audit confirmation: Labels passed pre-audit by French customs compliance institutions and EFSA pre-compliance review with zero revisions required.
Supplied full strain reports from EU-accredited laboratories:
1. QPS safety certification confirming strains as EU-approved safe organisms with no pathogenicity.
2. Third-party non-GMO test certificates verifying absence of exogenous gene insertion.
3. Genetic stability reports with 5-generation fermentation stability data confirming zero strain mutation.
Established a digital traceability system covering Raw Materials → Production → Finished Goods → Testing → Shipment → Customs Clearance → End Clients:
1. Unique traceable QR code assigned to every production batch.
2. QR code access to raw material purchase orders, fermentation records, enzyme activity test data, compliance documents, logistics delivery records and customs clearance status.
3. Two-way traceability integration with the client’s ERP system for real-time data queries.
Issued organic feed-specific enzyme certificates confirming zero chemical residues, non-GMO status and antibiotic-free production aligned with EU organic standards.
1. Pre-shipment simulated audit: Full document packages, labels and packaging submitted to French customs designated compliance institutions for mock clearance audits to identify and resolve risks in advance.
2. Pre-declaration of customs clearance documents: Electronic documents and traceability data submitted via EU ICS2 system 7 days prior to shipment for pre-clearance compliance review.
3. Dedicated full-cycle follow-up: HiSiaddi assigned bilingual French-English compliance officers to liaise directly with French customs, track clearance progress in real time and respond to audit inquiries immediately.
4. Emergency response protocols: Pre-established contingency plans for document revision, label replacement and traceability data supplementation with 24-hour response and 48-hour resolution timelines.
1. Authorization qualifications: Two EU-compliant manufacturers selected with products fully aligned with Regulation (EC) No 1831/2003 and filed on EU registration lists.
2. Document systems: 21 full English compliance documents fully covering EU audit checklists for one-pass approval.
3. Label & packaging: CLP-compliant English labels with traceable QR codes passing pre-audit with zero customs clearance objections.
4. Strain traceability: Non-GMO QPS strains + full-chain traceability systems enabling organic certification approval and end pasture acceptance.
A 12-ton batch of compound NSP enzymes shipped in February 2026 cleared French customs within 3 days with zero detention or objections. Parallel organic broiler diet trials conducted by the client verified stable enzyme activity, significant viscosity reduction, 3.5% FCR reduction and 40% mortality cut, fully meeting high-end organic breeding requirements.
The client designated HiSiaddi as its exclusive compliance service provider and core supplier with an annual procurement volume of 60 tons, additionally commissioning HiSiaddi as its dedicated EU compliance consultant to standardize compliance within its entire China supply chain and build a dedicated enzyme compliance audit system.
Quote from the Client Compliance Director: "HiSiaddi is the only partner in China with comprehensive expertise in EU feed enzyme compliance capable of systematic full-cycle problem resolution. Most Chinese manufacturers prioritize production over compliance, providing fragmented documents, non-standard labels and untraceable strains. HiSiaddi delivers full-cycle solutions aligned with EU standards covering qualification validation, document restructuring, label rectification, strain verification, traceability construction and customs clearance support, with professional English documentation and solid data enabling one-pass audit approval. They fully resolved our core bottlenecks of customs detention and organic certification failure, serving as our compliance cornerstone for expanding high-end enzyme supply chains from China."
For foreign mid-to-high-end clients purchasing compound NSP enzymes, compliance constitutes the primary threshold rather than pricing. Low-end buyers may accept incomplete documentation, Chinese-only labels and informal clearance channels, while mid-to-high-end EU clients must strictly adhere to Regulation (EC) No 1831/2003, CLP, FAMI-QS, non-GMO and full-traceability standards with zero violations, zero risks and full transparency.
HiSiaddi’s core competitive advantage lies in integrated three-in-one capacity: EU Compliance Expertise + Supply Chain Integration + Full-Cycle Implementation Services.
1. Professional barriers: Mastery of EU feed enzyme regulatory frameworks, EFSA audit key points, CLP labeling specifications and QPS strain requirements enabling precise compliance gap diagnosis and systematic remediation.
2. Resource barriers: Partnership with a small pool of domestic mid-to-high-end enzyme manufacturers holding full EU export qualifications, verified strain safety and standardized document systems for rapid qualification matching.
3. Service barriers: Closed-loop full-cycle service covering diagnosis, matching, restructuring, rectification, system construction and customs clearance support with full English documentation, traceable data, one-pass audit approval and zero customs detention guarantees.
Please contact HiSiaddi customer service for further inquiries regarding compound NSP enzyme compliance issues.
+86-13120989737 
info@hisiaddi.com 
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