About Keyshine Technology
Precision Chemistry, Trusted by Researchers Worldwide
Founded by scientists, built for science — Keyshine Technology has been delivering high-quality custom synthesis services to universities and research institutes since our founding.
Our Story
Built from the Bench Up
Keyshine Technology was founded by a team of experienced peptide and nucleic acid chemists who understood firsthand the challenges researchers face when sourcing high-quality custom synthesis services: inconsistent purity, missed deadlines, and inadequate documentation.
We set out to build a different kind of CRO and CDMO — one that combines the scientific rigor of an academic lab with the reliability and quality systems of a pharmaceutical manufacturer. Every project we take on is treated with the same care and precision we would apply to our own research.
Today, Keyshine Technology serves universities, national research institutes, and biotech companies across Asia and internationally, providing custom peptide synthesis, nucleic acid synthesis, and GMP-grade manufacturing services that researchers can depend on.
Scientific Integrity
We report results accurately and completely. If a synthesis presents challenges, we communicate proactively and work collaboratively to find solutions.
Uncompromising Quality
Every batch is fully characterized before release. We do not ship material that does not meet agreed specifications — no exceptions.
Researcher-First Partnership
We work with your timeline, your requirements, and your budget. Our scientists are available to discuss your project at every stage.
Continuous Improvement
We invest continuously in our analytical capabilities, synthesis infrastructure, and quality systems to stay at the forefront of the field.
Our team brings together deep expertise in synthetic chemistry, analytical science, and pharmaceutical development.
Our Facility
Purpose-Built for Precision Synthesis
Our facility is designed and operated to meet the demands of modern pharmaceutical research — from discovery-scale custom synthesis to GMP-grade manufacturing.
Quality Standards & Certifications
Our quality management system is built on internationally recognized standards and designed to support regulatory submissions worldwide.
GMP-Compliant Operations
Our manufacturing operations are conducted in accordance with ICH Q7 (Active Pharmaceutical Ingredients) and ICH Q11 (Development and Manufacture of Drug Substances) guidelines.
ISO-Aligned Quality System
Our quality management system is aligned with ISO standards for laboratory operations, including document control, change management, deviation handling, and CAPA processes.
Analytical Method Validation
All analytical methods used for product release are validated in accordance with ICH Q2(R1) guidelines for specificity, linearity, accuracy, precision, and robustness.
Data Integrity
We operate under ALCOA+ principles for data integrity — data is Attributable, Legible, Contemporaneous, Original, and Accurate, with full audit trails.
Supplier Qualification
All raw materials and reagents are sourced from qualified suppliers and undergo incoming quality control testing before use in synthesis.
Customer Audits Welcome
We welcome facility audits from customers and regulatory authorities. Our quality team will work with you to prepare audit documentation and facilitate on-site visits.
Partner with a Team That Takes Quality Seriously
Contact us to discuss your project requirements or to arrange a facility audit.