Dietary Supplement OEM / ODM for global brands
MITEYO — Dietary Supplement OEM / ODM
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QUALITY SYSTEM

Quality Control from Raw Materials to Batch Release.

Quality management is integrated with formula specifications, raw materials, manufacturing controls, packaging requirements, testing plans and batch documentation throughout commercial production.

MITEYO production team conducting an in-process manufacturing check
01

Quality control chain

Supplier QualificationMITEYO

Supplier Qualification

Qualified ingredient sources reviewed against specification, COA and project requirements.

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Incoming MaterialsMITEYO

Incoming Materials

Material identity, condition, lot information and incoming acceptance records.

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In-Process ControlsMITEYO

In-Process Controls

Dosage-form-specific checks during weighing, preparation, forming, filling and packaging.

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Finished ProductMITEYO

Finished Product

Appearance, count or weight and agreed project-specific tests.

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Packaging VerificationMITEYO

Packaging Verification

Artwork version, label, lot coding, seal integrity and case configuration.

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Batch ReleaseMITEYO

Batch Release

Record review, deviations, test status and release authorization.

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02

Testing Aligned with Product Specifications

Testing requirements depend on the dosage form, formula, customer requirements, destination market and agreed project specification. Qualified third-party testing is used where applicable.

Testing Aligned with Product Specifications
03

Traceability and records

Batch RecordsMITEYO

Batch Records

Production records connect materials, equipment, process checks and responsible operators to the relevant batch.

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Retained SamplesMITEYO

Retained Samples

Retained samples are identified by batch and managed according to applicable shelf-life and project requirements.

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Change ControlMITEYO

Change Control

Formula, supplier, process, artwork and packaging changes are reviewed and version-controlled before implementation.

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04

Certificates and documents

Review real certificate documents with clear holder, facility, scope and validity information on the certification page.

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