“Our founding principle was simple: every researcher and manufacturer deserves access to peptides of the highest purity, delivered with scientific transparency and commercial reliability.”
Dr. James ChenCo-Founder & Chief Scientific Officer
About PEPLYRAPioneering Peptide Science
Pioneering Peptide Science
Since 2004
A vertically integrated GMP manufacturer trusted by pharmaceutical, biotech, and cosmetic companies across 50+ countries — delivering precision, purity, and partnership.
20+Years of Excellence
1,200+Global Clients
50+Countries Served
40+Peptide Products
Two Decades of Peptide Innovation
From a small Hong Kong lab to a globally recognized GMP manufacturer — our journey has been defined by scientific rigor, client trust, and relentless innovation.
2004
Founded in Hong Kong
PEPLYRA was established by a team of MIT and Harvard biochemists with a mission to make high-purity peptides accessible to researchers worldwide.
2007
First GMP Certification
Achieved ISO 9001 and GMP certification for our first dedicated synthesis suite, enabling supply to regulated pharmaceutical clients.
2010
FDA Registration & Global Expansion
Registered with the U.S. FDA as an API manufacturer and began exporting to Europe, Japan, and Australia. Client base grew to 300+ companies.
2014
New 120,000 sq ft Campus
Opened our state-of-the-art manufacturing campus with 8 dedicated synthesis suites, analytical labs, and a cold-chain logistics center.
2018
OEM & Private Label Launch
Launched full-service OEM and private label programs, enabling brands to bring peptide-based products to market under their own identity.
2022
ICH Q7 Compliance & 50+ Countries
Achieved ICH Q7 compliance for API manufacturing and expanded distribution to 50+ countries, serving 1,200+ pharmaceutical and biotech clients.
2024
Next-Gen Peptide Platform
Launched our proprietary continuous-flow synthesis platform, reducing lead times by 40% and enabling production of complex long-chain peptides at commercial scale.
GMP Certifications &
Regulatory Compliance
Our quality systems meet the strictest international standards, giving partners confidence from research through commercial supply.
ISO 9001:2015
Quality Management System for Peptide Synthesis & API ManufacturingOur QMS covers the full lifecycle from raw material sourcing through final product release, ensuring consistent quality across all batches.
Certificate available upon request
HPLC Purity Analysis
≥98% purity guaranteed by RP-HPLC
Mass Spectrometry
ESI-MS and MALDI-TOF confirmation
Amino Acid Analysis
Full composition verification
Endotoxin Testing
LAL method, <1 EU/mg
Optical Rotation
Chiral purity confirmation
Full CoA Provided
Certificate of Analysis with every batch
120,000 sq ft of
World-Class Infrastructure
Our Hong Kong campus brings synthesis, analysis, formulation, and global cold-chain logistics together under one quality system.
01
Synthesis Suites
8 dedicated GMP synthesis suites with automated SPPS reactors, capable of producing from 1mg to 10kg per batch.
- 8 Synthesis Suites
- 1mg – 10kg Scale
- Automated SPPS
- Continuous-Flow Option
World-Class Scientists &
Industry Leaders
Our leadership team combines deep scientific expertise, manufacturing discipline, and global commercial experience.
20+ years in peptide chemistry and drug discovery. Former Principal Scientist at Pfizer. Author of 60+ peer-reviewed publications on solid-phase peptide synthesis and GLP-1 analogs.
Peptide ChemistryDrug DiscoveryGMP Compliance
15 years leading global pharmaceutical operations. Previously VP of Business Development at Lonza. Expert in scaling GMP manufacturing and building international distribution networks.
Business StrategyGlobal OperationsRegulatory Affairs
18 years in pharmaceutical QA/QC and regulatory submissions. Led FDA and EMA inspection readiness programs for 3 major API manufacturers. Expert in ICH Q7 and EU GMP Annex 11.
FDA ComplianceICH Q7Analytical Chemistry
12 years specializing in continuous-flow synthesis and scale-up chemistry. Developed proprietary synthesis protocols for 15+ commercial peptide APIs. Expert in complex long-chain peptide manufacturing.
Process ChemistryScale-upFlow Synthesis
10 years building pharmaceutical supply chain partnerships across North America, Europe, and Asia-Pacific. Manages relationships with 200+ key accounts including top-20 pharma companies.
Business DevelopmentKey AccountsSupply Chain
14 years in pharmaceutical formulation development and lyophilization. Expert in peptide stability, excipient selection, and sterile fill-finish operations for injectable and topical dosage forms.
FormulationLyophilizationSterile Fill-Finish
180+Team Members
60+PhD Scientists
200+Publications
35+Patents Filed
Partner With UsReady to Work With a
Ready to Work With a
Trusted GMP Partner?
Whether you need catalog peptides, custom synthesis, or full OEM support, our team is ready to help move your program forward.