Nerivanta Ingredients

以证据支撑的质量体系

Every batch is tested for identity, composition, oxidation, contaminants and microbiology, then released against the declared specification with its documentation attached.

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Illustrative photography: Analytical testing of retained ingredient samples

Release

Batch testing and release

Release is a decision, not a formality. Analytical data must match the agreed specification and the documents must be complete.

Batch release checks
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

Control points

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.

Documentation

The scope behind the document.

Confirm the issuing entity, product scope, validity and destination-market relevance for your selected grade.

GMPGMPPharmaceutical / API certificate

DMFDMFPharmaceutical / API regulatory file

CEPCEPPharmaceutical / API paper certificate

FSSCFSSC 22000Food safety system certificate

ISOISO 9001Quality management system

HACCPHACCPFood safety and hygiene control

IFOSIFOSInternational Fish Oil Standards test certificate

FOSFriend of the SeaSustainable sourcing certificate

GOEDGOEDGOED documentation and compliance

HALHalal / KosherHalal and Kosher certificates

FAMIFAMI-QSAnimal health and feed certificate

MOSHMOSH / MOAHMineral oil hydrocarbon test reports

Documentation categories for technical review. Availability, issuing entity, product scope and certificate validity require grade-specific confirmation.