Custom array & mold development
Patch contour, array geometry and tooling planning shaped around your development brief.
Explore capabilityCDMO · OEM · ODM · CRO · PRIVATE LABEL
Meet HYTANBIO: Hong Kong business coordination and Shaoxing manufacturing support for cosmetic microneedle patch development.
Cosmetic-oriented development. Feasibility, safety evidence and target-market classification guide every project.
Hytanbio Tech was founded in Hong Kong in 2026 to support global overseas business. Its in-house commercial production base, established in 2014, is located in Shaoxing, Mainland China.
The broader company platform includes a research center covering more than 4,000 square meters, peptide production lines, analytical and preparative HPLC systems, and clean laboratory infrastructure. This website focuses that platform on cosmetic-oriented dissolvable microneedle patch projects.
Our role is to connect formulation teams, skincare brands and distributors with an organized development and manufacturing pathway.

Patch contour, array geometry and tooling planning shaped around your development brief.
Explore capabilityCompatibility-led work on soluble matrices, peptides and market-appropriate cosmetic ingredients.
Explore capabilityA documented path through prototype review, mechanical screening, dissolution observations and pilot evaluation.
Explore capabilityPackaging, artwork, specifications and batch documentation connected to the scale-up plan.
Explore capabilityAn agreed brief sets the application, target market and evidence requirements. Each stage has an approval point so technical work and commercial planning stay aligned.
Application, target market, ingredient direction and commercial priorities.
Classification, array, formulation and testing requirements.
Review handling, appearance, structure and packaging fit.
Confirm agreed specifications and process consistency.
Finalize quality release, artwork, batch records and export coordination.
The company’s quality management approach follows ISO 9001:2015 principles. During supplier qualification, request current certificates, the named legal entity, covered site and product scope. A quality-system certificate does not by itself demonstrate a specific patch’s safety, efficacy or market approval.
Our project conversations cover specification confirmation, batch-wise quality documentation and export coordination. ISO 22716, GMP, microbiological or sterile claims must be supported by the documents and validated processes applicable to the product under discussion.
Share the application, ingredient direction, target market and expected volume. We’ll turn your brief into a clear development conversation.