جودة مدعومة بالأدلة
Every batch is tested for identity, composition, oxidation, contaminants and microbiology, then released against the declared specification with its documentation attached.
Batch testing and release
Release is a decision, not a formality. Analytical data must match the agreed specification and the documents must be complete.
| Identity | Fatty-acid profile by GC confirmed against the reference standard |
|---|---|
| Composition | EPA, DHA and total omega-3 verified against the declared specification |
| Oxidation | PV, AV and TOTOX compared with the declared release limit |
| Contaminants | Heavy metals, PCBs, dioxins, microbiology and MOSH/MOAH tested to destination limits |
| Documentation | COA, specification sheet and traceability record complete before dispatch |
Quality-control steps
Define the product, specification and target market.
Review the sample, analytical data and documentation.
Align packing, delivery and the release file before supply.
The scope behind the document.
Confirm the issuing entity, product scope, validity and destination-market relevance for your selected grade.
Documentation categories for technical review. Availability, issuing entity, product scope and certificate validity require grade-specific confirmation.
Download quality files
ملفات PDF أولية بالإنجليزية للمراجعة الداخلية فقط. بيانات الشركة والمواصفات والمؤهلات غير مؤكدة، ولم يُعتمد توزيعها خارجياً.
نبذة عن الشركة
تعريف بالعلامة والفئات المقترحة وآلية مراجعة المشاريع.
Nerivanta-Company-Profile.pdfقائمة مواصفات المنتجات
بيانات منتجات مرجعية وقائمة للاستفسارات؛ القيم بحاجة إلى التحقق.
Nerivanta-Product-Specification-List.pdfالجودة والوثائق
إطار لمراجعة الجودة وقائمة الوثائق؛ ليست شهادة أو تقرير اختبار.
Nerivanta-Quality-Documentation.pdfRequest certificates
Send the product, specification and destination market. We reply with the certificate set and batch documentation.