---
name: Global Biotech Laboratories
slug: globalbiotechlaboratories
site: cdmo
website_domain: globalbiotechlaboratories.com
summary: Global Biotech Laboratories is a peptide and oligonucleotide CDMO offering end-to-end contract development and manufacturing from route scouting through validated commercial supply, with cGMP and ICH Q7 compliance across manufacturing sites on three continents. Headquartered in Boston, United States.
tagline: End-to-end peptide and oligonucleotide CDMO with cGMP manufacturing and global cold-chain logistics.
founded_year: 
employee_count_band: 
employee_count_label: 
parent_name: 
parent_slug: 
hq_country: US
tier2_domain_verified: false
updated_at: 2026-08-16T07:00:50.162Z
services_count: 11
modalities_count: 2
indications_count: 0
locations_count: 6
review_signal_gate: closed
generated_by: BioBM Editorial AI
---

# Global Biotech Laboratories

End-to-end peptide and oligonucleotide CDMO with cGMP manufacturing and global cold-chain logistics.

Listed on cdmo.directory.

## Summary

Global Biotech Laboratories is a peptide and oligonucleotide CDMO offering end-to-end contract development and manufacturing from route scouting through validated commercial supply, with cGMP and ICH Q7 compliance across manufacturing sites on three continents. Headquartered in Boston, United States.

## At a glance

- HQ country: US

## Services

- Peptide Manufacturing
- Oligonucleotide Manufacturing
- Process Development
- CMC Analytical Development
- Formulation Development
- Stability Testing & Storage
- Quality Control Testing
- Technology Transfer
- CMC Regulatory Submission Support
- API Synthesis & Manufacturing
- Cold-Chain Storage & Logistics

## Modalities

- Peptide
- Oligonucleotide

## Locations

- Boston, Boston, Massachusetts, United States
- San Diego, San Diego, California, United States
- Basel, Basel, Basel-Stadt, Switzerland
- Dublin, Dublin, Dublin, Ireland
- Singapore, Singapore, Singapore, Singapore
- Tokyo, Tokyo, Tokyo, Japan

## Certifications

- ISO; Identifier: ISO 9001:2015; Source: https://globalbiotechlaboratories.com/
- ISO; Identifier: ISO 13485; Source: https://globalbiotechlaboratories.com/
- FDA; Identifier: FDA Registered; Source: https://globalbiotechlaboratories.com/
- EMA; Identifier: EMA Compliant; Source: https://globalbiotechlaboratories.com/
- ICH; Identifier: ICH Q7; Source: https://globalbiotechlaboratories.com/

## Long description

## Overview

Global Biotech Laboratories (GBL) is a contract development and manufacturing organization (CDMO) specializing in peptides, oligonucleotides, and complex biomolecules. The company operates under cGMP and ICH Q7 standards across manufacturing hubs in North America (Boston, San Diego), Europe (Basel, Dublin), and Asia-Pacific (Singapore, Tokyo).

## Core Services

**Peptide Manufacturing & Synthesis**
- Custom peptide synthesis from milligram research quantities to multi-kilogram commercial scale
- Solid-phase and solution-phase synthesis with decades of process expertise
- GMP peptide active pharmaceutical ingredients (APIs) with controlled impurity profiles and stability support
- Phase-appropriate GMP manufacturing from first clinical batch through validated commercial supply

**Oligonucleotides**
- Therapeutic and diagnostic oligonucleotide manufacturing with rigorous purification and analytics
- Full traceability for next-generation modalities

**CDMO Services**
- End-to-end contract development and manufacturing: route scouting, process development, analytical development, scale-up, validation, and tech transfer
- Regulatory and CMC documentation support for IND/IMPD and commercial filings
- Engagement models for generic APIs, custom synthesis, clinical/commercial programs, and research supply

**Analytical Sciences**
- Method development and validation (HPLC, MS, orthogonal methods)
- Stability studies and release testing
- Characterization and quality control

**Catalog & Reagents**
- Over 1,400 high-purity building blocks, generic peptides, and reference standards
- Same-week global dispatch

**Global Distribution**
- Temperature-controlled, validated cold-chain logistics with real-time tracking
- Reach to 62 countries with 24/7 follow-the-sun support

## Quality & Compliance

- cGMP and ICH Q7 operations across all sites
- ISO 9001:2015 and ISO 13485 certified
- FDA registered and EMA compliant
- USP & EP standards
- ALCOA+ data integrity principles
- Audit-ready documentation and batch records
- Flawless inspection history
- Quality by Design (QbD) principles embedded in process development

## Differentiation

- Integrated development, analytics, and manufacturing under one quality system
- Process innovation focused on green chemistry, higher yields, and reduced cost of goods
- Expertise in conjugates, lipidated peptides, and complex oligonucleotides
- Dual-sourcing strategies and supply assurance with 99% on-time delivery
- Seamless scale-up from research through commercial phases

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- [Biospring](/companies/biospring) (Oligonucleotide Manufacturing, Process Development) — [Compare](/compare/biospring/globalbiotechlaboratories)

_Profile last updated: 2026-08-16T07:00:50.162Z. Profile facts may include AI-assisted enrichment._

Auto-generated by BioBM Editorial AI for machine-readable profile access.