
Co-manufacturing system
Production is carried out by co-manufacturing sites, covering powders, staple food, grooming and cleaning formats.
MANUFACTURING & QUALITY
A verifiable manufacturing and quality framework that supports stable supply for the cat-allergen management category.
Production runs through a co-manufacturing system covering powders, baked staple food, grooming and cleaning formats. Quality control moves in three stages: raw material, in-process and finished product. All statements on capacity, certification and testing follow verified information only.

MANUFACTURING

Production is carried out by co-manufacturing sites, covering powders, staple food, grooming and cleaning formats.

Standardized clean workshops and supporting automated lines are used for consistent production across formats.

Equipment such as low-temperature jet milling and microwave sterilisation serves raw-material processing and format stability.

Covering powders, baked staple food, grooming and cleaning categories; selectable formats depend on project and production schedule.
QUALITY CONTROL
Incoming materials are inspected and recorded against defined standards; non-conforming lots do not enter production.
In-process checks and records at key production points support format consistency.
Finished products are tested against project-defined indicators and retained as samples, with records archived by batch.
R&D PLATFORM
R&D works across molecular targets, IgY ingredients, pet nutrition and dosage-form translation, and brings real household use into validation. Every external citation and conclusion follows published literature or verified test conditions.
DOCUMENTATION
We do not pre-claim any certification or test conclusion we have not obtained. The available document types are confirmed after project verification and typically include product overview, specification, ingredient and usage information, storage and shelf-life information, and other documents on request.

MANUFACTURING FAQ
Public statements follow verified information; unverified capacity or output figures are not published in advance. Specific capability is discussed within the project.
Certification documents can be provided after project verification.
Raw-material inspection, in-process checks and finished-product testing records are archived by batch, forming a traceable quality document chain.
MANUFACTURING & QUALITY
We do not pre-claim any certification or test conclusion we have not obtained. The available document types are confirmed after project verification and typically include product overview, specification, ingredient and usage information, storage and shelf-life information, and other documents on request.