Reliable testing and clear documentation are critical for regulatory compliance and brand reputation. We combine in-house controls with flexible third-party testing options.
We offer multiple testing options to meet your specific market requirements and quality standards.
Standard
Every batch is produced under GMP with defined specifications. As standard, we provide:
Where appropriate, we also cooperate with accredited laboratories in China to perform independent testing.
On Request
For additional assurance or specific test items, we can coordinate testing with accredited third-party laboratories in China.
Results are issued as independent COAs that complement our internal documentation.
Premium Option
For certain markets or flagship products, you may prefer testing from a laboratory in Australia.
This is an optional service with fees quoted separately.
Depending on your project, we can support you with comprehensive documentation to meet regulatory and market requirements.
Finished product COAs and specifications with complete analytical data
Complete raw material documentation packages with traceability
Allergen and non-GMO statements for your market requirements
Basic stability information where available for shelf-life determination
Manufacturing and quality-related statements for regulatory reviews
Supportive documentation for structure/function claim substantiation
We are not a regulatory authority or law firm, but we understand what most importers, platforms and inspectors expect in practice. Our documentation packages are designed to meet common requirements across major markets.
Whether you choose standard China OEM or hybrid manufacturing, we’re here to support your nutraceutical brand development.
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