About Hytanbio Tech
Hytanbio Tech connects Hong Kong-based international R&D and project coordination with an established peptide manufacturing base in Shaoxing, Mainland China.
Hytanbio Tech connects Hong Kong-based international R&D and project coordination with an established peptide manufacturing base in Shaoxing, Mainland China.
Founded in 2026 in Hong Kong, Hytanbio Tech is a biological R&D entity established specifically to support global overseas business expansion.
Our in-house large-scale commercial manufacturing facility was founded in 2014 and is located in Shaoxing, Mainland China. Together, the Hong Kong organization and Mainland production base connect international project coordination with established peptide manufacturing infrastructure.
Backed by an R&D center covering more than 4,000 square meters, we operate multiple complete peptide production lines with large-scale peptide synthesizers, imported advanced HPLC analytical and preparative systems, and GMP-standard clean laboratories. Our quality management system is certified to ISO 9001:2015, supporting stable product quality, controlled documentation and regulatory traceability.
Our core commercial specialization is cosmetic-grade peptide raw materials and innovative cosmetic delivery systems. The portfolio includes peptide raw materials, lyophilized peptide powder, dissolvable microneedle patches, dissolvable oral films and full-chain OEM / ODM private-label services.
Hytanbio Tech was founded in Hong Kong for international business and R&D coordination.
Our in-house commercial manufacturing facility was established in Shaoxing.
Dedicated peptide R&D infrastructure for synthesis, purification, analysis and process development.
A certified quality management system supports consistency, documentation control and traceability.
Our scientist-led technical team combines peptide research, pilot trials, analytical development and scalable manufacturing. The operating model is designed to turn an early technical brief into a documented, export-ready B2B project.
Our service architecture combines peptide manufacturing with formulation, delivery-system and private-label execution, giving global buyers one accountable path from technical evaluation to commercial supply.
Cosmetic-oriented peptide ingredients supplied against an agreed identity, specification and documentation package.
Freeze-dried bulk powder, custom blends and vial formats developed around stability, handling and commercial requirements.
Delivery-system development support for dissolvable cosmetic microneedle patch concepts and private-label programs.
Film-formulation and manufacturing coordination for qualified development programs and market-specific product pathways.
Sequence review, synthesis, modification, purification and analytical support from research quantity through scale-up.
Feasibility assessment, prototype sampling and compatibility-led development for innovative cosmetic formats.
Full-chain support covering formula, vial or delivery format, pilot production, packaging and commercial manufacture.
Specification alignment, batch-wise quality documents, packaging review and global export coordination.
Every project is evaluated against its intended use, product grade, destination market and required quality package. Current approved specifications and batch documents take precedence over general website information.
We bridge laboratory-scale R&D and full commercial-volume manufacturing through a coordinated technical and commercial workflow.
Our integrated OEM workflow connects requirement discovery, targeted development, sampling, packaging design and approved commercial production.

We work with organizations that need a stable, traceable supply partner and a clear route from product selection to commercial execution.
Share the target material, format, quantity range, packaging concept, destination market and required documentation. Our team will map the next technical and commercial steps.