---
name: Dalton Pharma Services
slug: dalton
site: cdmo
website_domain: dalton.com
summary: Health Canada–approved and FDA-inspected cGMP contract manufacturer offering integrated drug discovery, development, and manufacturing services including custom synthesis, API production, formulation development, and sterile fill-finish for vials, syringes, and cartridges. Headquartered in Toronto, Canada.
tagline: Integrated drug discovery, development, and cGMP manufacturing—35+ years of expertise in custom synthesis, API production, and sterile fill-finish.
founded_year: 1986
employee_count_band: 
employee_count_label: 
parent_name: 
parent_slug: 
hq_country: CA
tier2_domain_verified: false
updated_at: 2026-08-16T07:01:02.224Z
services_count: 17
modalities_count: 3
indications_count: 2
locations_count: 1
review_signal_gate: closed
generated_by: BioBM Editorial AI
---

# Dalton Pharma Services

Integrated drug discovery, development, and cGMP manufacturing—35+ years of expertise in custom synthesis, API production, and sterile fill-finish.

Listed on cdmo.directory.

## Summary

Health Canada–approved and FDA-inspected cGMP contract manufacturer offering integrated drug discovery, development, and manufacturing services including custom synthesis, API production, formulation development, and sterile fill-finish for vials, syringes, and cartridges. Headquartered in Toronto, Canada.

## At a glance

- Founded: 1986
- HQ country: CA

## Services

- CMC Analytical Development
- Formulation Development
- Process Development
- API Synthesis & Manufacturing
- HPAPI Manufacturing (High-Potency)
- Small Molecule Development & Manufacturing
- Vial Filling
- Prefilled Syringe (PFS) Filling
- Cartridge Filling
- Sterile Fill-Finish & Aseptic Manufacturing
- Lyophilization (Freeze Drying)
- Stability Testing & Storage
- Extractables & Leachables Studies
- Quality Control Testing
- Flow Chemistry & Continuous Manufacturing
- Oligonucleotide Manufacturing
- Bioconjugation Services

## Modalities

- Small Molecule
- Peptide
- Oligonucleotide

## Indications

- Oncology
- Nephrology

## Locations

- Headquarters & Manufacturing, Toronto, Ontario, Canada

## Certifications

- Health Canada; Identifier: Health Canada Establishment License; Source: https://dalton.com/pharmaceutical-development-manufacturing-services
- Health Canada; Identifier: Cannabis Analytical Test Licence; Source: https://dalton.com/

## Long description

## Overview

Dalton Pharma Services is a leading pharmaceutical contract development and manufacturing organization (CDMO) headquartered in Toronto, Canada. Since its formation in 1986, the company has provided integrated chemistry, drug development, and manufacturing services to pharmaceutical and biotechnology clients globally. The organization is Health Canada–approved and FDA-inspected, with over 35 years of experience emphasizing quality, speed, and flexibility.

## Core Capabilities

**Discovery & Development:**
- Medicinal chemistry and contract research
- Polymorphic screening and synthetic feasibility analysis
- Synthetic route development and process optimization
- Conjugation services and scale-up of difficult chemistry
- Analytical development (accelerated stability testing, ICP-MS, UPLC, extractables & leachables)
- Drug analogue development

**Manufacturing:**
- cGMP API manufacturing and sterile API manufacturing
- API process development and reaction optimization
- Formulation development (including liposomal formulations and sterile formulations)
- Custom chemical synthesis in multi-kilo batches (22 L to 250 L glass reactors)
- Flow chemistry and hydrogenation capabilities
- cGMP oligonucleotide fill services

**Fill-Finish Services:**
- cGMP aseptic filling (liquid and powder)
- Sterile vial filling (including automated Capmatic Patriot® system and RoboFil™ aseptic powder fill-finish)
- Prefilled syringe and cartridge filling
- Isolator-based aseptic technology

## Facilities & Infrastructure

The Toronto facility underwent significant upgrade and expansion in 2016, featuring:
- Approximately 2,500 sq ft (232 sq m) cGMP manufacturing area with Grade C classification
- Two GMP suites equipped with stainless steel tables, 8-foot walk-in hoods, and 6-foot bench-top fume hoods
- Aseptic filling area (~300 sq ft) with Grade A localized environment under Restricted Access Barrier Systems (RABs)
- New HEPA systems, vial washing-depyrogenation capabilities, and WFI system (Steris, qualified 2014)
- Autoclave room with Class A environment
- Two synthetic laboratories (~1,100 sq ft each) for R&D
- Hydrogenation room with 2 × 2 L Parr reactors
- Building Automation System monitoring temperature, humidity, and pressurization
- Security system with proximity card access and surveillance cameras

## Regulatory & Recognition

- Health Canada Establishment License holder
- FDA-inspected facility
- CMO Leadership Awards (2016, 2017, 2018) from Life Science Leader in Quality, Reliability, Capabilities, Expertise, Compatibility, and Development
- Cannabis Analytical Test Licence from Health Canada (under Cannabis Act and Regulations)

## Business Model

Privately held and self-funded. The company operates as a full-service CDMO with integrated capabilities allowing clients to accelerate drug discovery and development programs by consolidating process development, API manufacturing, and finished-dose manufacturing at a single location.

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_Profile last updated: 2026-08-16T07:01:02.224Z. Profile facts may include AI-assisted enrichment._

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