NSF cGMP
Review this document’s named holder, facility scope and current validity. Confirm applicability to the proposed formula and production route.
SLEEPStart Your ProjectOur Shenzhen team handles sales and R&D; the manufacturing facility handles production. We connect buyer requirements with formula, sample, packaging and production review.

MITEYO’s Shenzhen team handles sales and research and development. Production is handled by the manufacturing facility. Project review connects the product brief, sampling, production requirements and applicable documentation.
MITEYO’s Shenzhen team handles sales and research and development. Production is handled by the manufacturing facility. Project review connects the product brief, sampling, production requirements and applicable documentation.
Supplier qualification should identify the contracting and production entities, relevant facility scope and the documents applicable to the order. No ownership, exclusivity or blanket certification relationship is implied.

Review current manufacturing certifications by certification name and practical role in manufacturing, quality management and customer qualification. Detailed certificate documents can be opened from each certification item.
Review this document’s named holder, facility scope and current validity. Confirm applicability to the proposed formula and production route.
Review the registered facility and applicable scope. Facility registration is not FDA approval of a product.
Review this document’s named holder, facility scope and current validity. Confirm applicability to the proposed formula and production route.
Review this document’s named holder, facility scope and current validity. Confirm applicability to the proposed formula and production route.
ISO 22000:2018 food-safety management document naming GUANGDONG COME HEALTH BIOTECHNOLOGY CO.,LTD. Verify its facility scope and current validity for the proposed project.
Our team meets buyers at international industry events to review product samples, packaging, dosage forms and OEM/ODM project requirements.












MITEYO’s Shenzhen team handles sales and research and development. Production is handled by the manufacturing facility. Project review connects the product brief, sampling, production requirements and applicable documentation.
Start with the essentials. Our Shenzhen sales and R&D team coordinates feasibility and commercial review with the production facility.
Your submitted contact and project details are stored in the website inquiry system for MITEYO team follow-up. The submitted page, product context, referrer and campaign parameters may be included to help us understand your request. This form does not automatically send a WhatsApp message. Choosing WhatsApp opens that separate service.
For questions about information you have submitted, contact emma@miteyobio.com.