Product illustrationHytanbio Tech · Peptide CDMO Partner
Peptide CDMO Services From Sequence to Commercial Scale
Scientist-led development, process scale-up, analytical support and manufacturing coordination for complex peptide programs.
OEM · ODM · CRO · CDMOISO 9001 · ISO 22000HACCP · GMP
4,000 m²+R&D center
Since 2014Commercial manufacturing base
Multiple linesPeptide production and scale-up
Global projectsExport and documentation coordination
Six integrated service lines
One technical partner across the peptide program
Each project starts with identity, intended use, quality target, scale and documentation needs. Scope, methods, capacity and lead time are confirmed in the written proposal.
Custom Peptide Synthesis
Linear, cyclic, modified, labeled and project-specific peptides from feasibility review through analytical release.
Learn more →Process Development & Scale-Up
Route optimization, impurity review, pilot work and transfer planning for larger campaigns.
Learn more →Lyophilized Peptide CDMO
Formulation, lyophilization cycle review, vial presentation, packaging and project documentation.
Learn more →Peptide Intermediates
Protected amino acids, peptide fragments, linkers, resins and related synthesis inputs.
Learn more →Cosmetic Peptide CDMO
Cosmetic-grade peptide programs, formulation development and delivery-system OEM / ODM.
Learn more →Analytical Testing
Project-scoped HPLC, MS and other analytical or documentation requirements reviewed before quotation.
Learn more →End-to-end delivery framework
Eight gates from project brief to ongoing supply
Deliverables and decision points remain visible across development, pilot and manufacturing phases.
Project Brief
Sequence, identity, use, scale and destination.
Feasibility Review
Technical fit, risk and analytical scope.
Process Development
Route, conditions and impurity strategy.
Pilot Production
Representative scale and process learning.
Analytical QC
Agreed methods and acceptance criteria.
Scale-Up Manufacturing
Campaign planning and controlled execution.
Documentation & Release
Batch-specific review and release package.
After-Sales Support
Deviation, repeat-order and supply coordination.
Development and manufacturing platform
Built to bridge laboratory work and commercial programs
4,000 m²+R&D center
Project feasibility, development and analytical work.
2014Manufacturing base
Shaoxing in-house production operations.
HPLC / MSAnalytical support
Methods and criteria scoped by project.
mg → kgScale planning
Feasibility varies by sequence and specification.
Quality and compliance
Certified systems, project-specific evidence
Hytanbio reports ISO 9001, ISO 22000, HACCP and GMP certifications. Certificate numbers, issuing bodies, covered legal entity, scope and validity are reviewed against current originals. Product acceptance remains tied to the signed specification and relevant batch documents.
ISO 9001Quality management
ISO 22000Food safety management
HACCPHazard control system
GMPManufacturing controls
Source-grounded product catalog
Browse all products →Peptide materials available for CDMO review
Browse 1,132 cleaned catalog identities from the supplied product workbook. Every listed material can be discussed for OEM, ODM, CRO or CDMO scope; current specification, availability and documents require project confirmation.
Beyond peptide synthesis
OEM and ODM for peptide powders and delivery systems
Our portfolio includes lyophilized peptide powder, cosmetic peptide materials, dissolvable microneedle patches, oral films and related packaging concepts. A visual is a development reference, not proof of a released product or current batch.
- Feasibility and formula review
- Prototype and sample planning
- Specification and packaging alignment
- Batch documentation and export coordination
Start with a precise project brief
Send the sequence or material identity, modification, quantity, target specification, intended application, required documents and destination market.
Request Project Quote →