Quality & Compliance

Quality planning for raw materials, production controls, COA, third-party testing and retail files.

What buyers need to confirm

Raw-material specification and identity review
In-process checks during filling, compression, coating or packing
Microbiology, heavy metals and active marker testing as agreed
COA and third-party testing support
Project documentation aligned before production

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Verified planning workflow

How this scope is defined.

Raw-material specification and supplier-file review
In-process weight, appearance and line checks
Packaging and coding verification
Finished-product tests according to the agreed specification
COA, third-party reports and release documents by scope

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Buyer FAQ

Is every test included by default?

No. The formula, dosage form, destination market and quotation define which tests are included and which are optional.

What is the difference between a COA and third-party testing?

A COA reports results against an agreed specification. Third-party testing is performed by an external laboratory and must be separately scoped when required.

Are supplements FDA approved?

Dietary supplements should not be described as FDA approved. Facility, manufacturing, labeling and product responsibilities must be represented accurately.