Peptide Oral Dissolving Film · B2B
Oral Dissolving Film Technology
Uniform thin-film design with controlled thickness, handling and disintegration targets.
Content updated · Evidence and updates
Hytanbio Tech was founded in Hong Kong in 2026 to support overseas business, according to the company profile supplied for this website. The same profile identifies an in-house manufacturing base established in Shaoxing in 2014 and a research center covering more than 4,000 square meters. These dates describe different entities and facilities; they should not be presented as the same incorporation date. The listed capabilities include peptide development, analytical and preparative HPLC, film development and packaging coordination. For supplier qualification, request documents identifying the legal entity, operating site and activities included in the proposed order. A photograph or certificate montage is an overview, not a substitute for a readable current certificate and its scope. Specific oral-film capacity, validated product parameters and commercial timelines should be confirmed in project documentation rather than inferred from research-center floor area.
A Hong Kong–based biological R&D company connecting peptide science, delivery-system development and commercial manufacturing for global partners.
Founded in 2026 in Hong Kong, Hytanbio Tech was established specifically to support international business development. Our large-scale commercial manufacturing facility, founded in 2014 and located in Shaoxing, Mainland China, operates as our in-house production base.
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 framework follows ISO 9001:2015 requirements to support consistent product quality and regulatory traceability.
We specialize in cosmetic-grade peptide raw materials and innovative cosmetic delivery systems. Our portfolio includes peptide raw materials, lyophilized peptide powder, dissolvable microneedle patches, dissolvable oral films, and full-chain OEM / ODM private-label services.
By bridging laboratory R&D with commercial-volume manufacturing, we provide formula feasibility assessment, prototype sampling, specification confirmation, batch-level quality documentation, packaging coordination and global export support.
Our scientist-led technical team integrates peptide research, pilot trials and mass production to serve skincare brands, cosmetic laboratories, beauty institutions and cross-border distributors with stable, traceable and market-oriented solutions.
Hong Kong entity established for global business development.
In-house commercial manufacturing base located in Shaoxing.
Dedicated facilities supporting peptide and delivery-system development.
Integrated technical, quality, packaging and export coordination.
Our technical platform connects formulation science with scalable production. Projects move through a documented path from feasibility review and laboratory sampling to pilot validation, commercial manufacturing and shipment preparation.
Large-scale peptide synthesis, HPLC analysis and purification, GMP-standard clean laboratories and batch-wise quality documentation support consistent execution across development stages.
One technical platform for peptide ingredients, innovative delivery formats and private-label commercialization.
Cosmetic-grade peptide ingredients supported by specification and quality-document planning.
Freeze-dried peptide formats developed around stability, handling and project requirements.
Thin-film formulation, sensory optimization, unit-dose packaging and scalable manufacturing.
Innovative cosmetic delivery-system development from concept through prototype validation.
Formula feasibility, sampling, specifications, artwork, packaging and commercial production.
Batch-wise documentation and destination-market export coordination for B2B projects.
Our manufacturing and quality framework is supported by documented systems and qualifications covering quality management, food safety, GMP-related controls and export compliance. Certification scope and current validity can be provided during project due diligence.

We begin with the destination market and target product profile, define measurable quality attributes, and then progress through prototypes, specifications, scale-up and packaging with documented decisions.
We work with skincare brands, cosmetic laboratories, beauty institutions, wellness companies and cross-border distributors seeking a technically grounded OEM / ODM partner.
Share your target market, dosage form, ingredient concept and estimated volume for an initial feasibility review.
HYTAN BIO TECH presents an oral film business combining research, manufacturing and sales support in its October 2026 brochure. The supplied materials show production areas, automated equipment, a testing center, air-shower access and water-treatment support. These descriptions complement the company background on this page, including the distinction between the Hong Kong business entity and its Mainland China manufacturing base. The brochure also reports platform-level capacity and staffing figures. Those figures are supplier-provided references, not a reserved production allocation, a batch release record or proof of a particular product specification. Buyers should confirm the contracting entity, manufacturing site and scope of work during supplier qualification. Request current documentation for the actual facility and intended product category, then connect the approved sample, technical specification and production responsibilities in the project agreement.
| Brochure-reported reference | Value in supplied edition | Confirmation needed |
|---|---|---|
| Designed daily output | 2 million films | Site, product mix and available allocation |
| Annual capacity | More than 600 million films | Design basis and applicable production scope |
| Automated high-speed lines | 4 | Current configuration and product applicability |
| Cleanroom reference | Class 100,000 | Applicable classification and current records |
| R&D and production staff | 200+ | Current staffing scope |
| Standard-order dispatch | Within 20 days | Agreed start point, materials and order conditions |
Capacity, staffing and dispatch references above come from brochure pages 3-4. Confirm current supporting records and project applicability before relying on them.







Original facility photographs supplied in brochure page 3, displayed in their natural colors. Confirm the site identity and current facility scope during supplier qualification.