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Leading CDMO Companies in Canada

Your Trusted Canadian Partners for Pharmaceutical Development and Manufacturing

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Pharmaron API Commercial Synthesis Coventry (US)
United States

Pharmaron API Commercial Synthesis Coventry (US)

Pharmaron

Commercial API Small Molecules Synthesis.

BATCH SIZE: Small, Medium, Large

THERAPEUTIC AREAS OF EXPERTISE (ATC): (R) Respiratory system, (H) Systemic hormonal preparations excl. sex hormones and insulins, (V01) Allergens, (M) Musculoskeletal system, (L) Antineoplastic and immunomodulating agents, (V04) Diagnostic agents, (S) Sensory organs, (G) Genito urinary system and sex hormones, (J) Antiinfectives for systemic use, (C) Cardiovascular system, (A) Digestive tract and metabolism, (D) Dermatologicals, (N) Nervous system, (P) Antiparasitic products, insecticides and repellents, (B) Blood and blood forming organs, (V06) Nutrients

CONTROLLED SUBSTANCES: Lowest potential for abuse, High potential for abuse & no medical use, High potential for abuse & medical use, Lower potential for abuse, Low potential for abuse

USE: Human, Veterinary

MARKETS: PMDA (Japan), FDA (USA), EMA (EU), MFDS (South Korea), TGA (Australia), Health Canada (Canada), MHRA (UK)

OEB (Occupational Exposure Banding): 2 (PDE = 1,000 - 10,000 µg/day), 4 / HPAPI (PDE = 10 - 100 µg/day), 1 / low-hazard (PDE > 10,000 µg/day), 3 (PDE = 100 - 1,000 µg/day)

SERVICES: Manufacturing services, Development services

REGION: North America

COMPLIANCE: FDA (cGMP), ECOVADIS, ISO

CATEGORY / PRODUCT: CHEMICAL-SYNTHETIC

Lifecore Injectables CDMO
United States

Lifecore Injectables CDMO

Lifecore Biomedical

CDMO that manufactures clinical & commercial sterile injectable drug products.

MARKETS: DIGEMID (Peru), ANMAT (Argentina), Turkish Health Authorities, EDE (UAE), Rest of World, ANVISA (Brazil), ISP (Chile), PMDA (Japan), FDA (USA), MSPAS (Guatemala), CDSCO (India), Russian Health Authorities, EMA (EU), COFEPRIS (Mexico), MFDS (South Korea), SFDA (Saudi Arabia), TGA (Australia), NMPA (China), Health Canada (Canada), INVIMA (Colombia), MHRA (UK)

BATCH SIZE: Small, Medium, Large

CATEGORY / PRODUCT: FDF / DRUG PRODUCTS

COMPLIANCE: EMA (EU GMP), ANVISA (Brazil B-GMP), TGA (Australia GMP), FDA (cGMP), ECOVADIS, ISO, Health Canada (Canada GMP), MFDS/KFDA (Republic of Korea GMP)

CONTROLLED SUBSTANCES: Lowest potential for abuse

BSL (Biological Safety Level): 3, 1, 2

USE: Human, Veterinary

SERVICES: Analytical / QC services, Logistics, Manufacturing services, Regulatory services, Development services, Packaging, Quality Assurance services

OEB (Occupational Exposure Banding): 2 (PDE = 1,000 - 10,000 µg/day), 4 / HPAPI (PDE = 10 - 100 µg/day), 1 / low-hazard (PDE > 10,000 µg/day), 3 (PDE = 100 - 1,000 µg/day)

REGION: North America

Aenova Group - Location Greensboro, USA
United States

Aenova Group - Location Greensboro, USA

Aenova

Competence Center Packaging Solids.

BATCH SIZE: Small, Medium, Large

USE: Human

SERVICES: Logistics, Manufacturing services, Packaging

REGION: North America

MARKETS: FDA (USA), Health Canada (Canada)

COMPLIANCE: FDA (cGMP), NSF, Halal Research Council, Health Canada (Canada GMP)

CATEGORY / PRODUCT: NUTRACEUTICALS

Adare Pharma | US
United States

Adare Pharma | US

Adare Pharma Solutions

Adare Pharma es un CDMO global con instalaciones en EE.UU. y la UE, que ofrece desarrollo de productos llave en mano mediante experiencia en fabricación comerci

MARKETS: DIGEMID (Peru), ANMAT (Argentina), EDE (UAE), ANVISA (Brazil), ISP (Chile), PMDA (Japan), FDA (USA), MSPAS (Guatemala), Russian Health Authorities, EMA (EU), COFEPRIS (Mexico), MFDS (South Korea), SFDA (Saudi Arabia), TGA (Australia), NMPA (China), Health Canada (Canada), INVIMA (Colombia), MHRA (UK)

BATCH SIZE: Small, Medium, Large

CATEGORY / PRODUCT: FDF / DRUG PRODUCTS, SERVICES, PARTICLE ENGINEERING

COMPLIANCE: EMA (EU GMP), PMDA/MHLW (Japan GMP), UAE Ministry of Health & Prevention, ANVISA (Brazil B-GMP), World Health Organization (GMP / HACCP), MHRA (UK GMP), French Service-Public (CIR), TGA (Australia GMP), FDA (cGMP), NMPA (China GMP), ECOVADIS, ISO, Halal Research Council, Health Canada (Canada GMP), TITCK (Turkish Health Authorities), MFDS/KFDA (Republic of Korea GMP)

USE: Human, Veterinary

SERVICES: Analytical / QC services, Logistics, Manufacturing services, Regulatory services, Development services, Packaging, Quality Assurance services

OEB (Occupational Exposure Banding): 2 (PDE = 1,000 - 10,000 µg/day), 4 / HPAPI (PDE = 10 - 100 µg/day), 1 / low-hazard (PDE > 10,000 µg/day), 3 (PDE = 100 - 1,000 µg/day)

REGION: North America

THERAPEUTIC AREAS OF EXPERTISE (ATC): (C) Cardiovascular system, (A) Digestive tract and metabolism

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FDF / DRUG PRODUCTS manufacturing site

MAI network supplier

Contract Development and Manufacturing Organization (CDMO) with a focus on recombinant proteins and monoclonal antibodies (mAbs).

Location available after registration

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CHEMICAL-SYNTHETIC manufacturing site

MAI network supplier

BOC Science Plants

Location available after registration

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FDF / DRUG PRODUCTS manufacturing site

MAI network supplier

CDMO specializing in sterile unit-dose liquid drug products using Blow-Fill-Seal (BFS) technology for ophthalmic, nasal and inhalation therapies.

Location available after registration

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CDMO/CMO facility

MAI network supplier

Headquarters

Location available after registration

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CDMO/CMO facility

MAI network supplier

Creative Proteomics Cytokine provides comprehensive cytokine analysis services for immune research, biomarker discovery, and pharmaceutical development. Using advanced Luminex multiplex assays and…

Location available after registration

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CDMO/CMO facility

MAI network supplier

global life science service provider

Location available after registration

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FDF / DRUG PRODUCTS manufacturing site

MAI network supplier

Lannetts main manufacturing site sits in Seymour, Indiana, and includes capabilities for Oral Solid Dose (OSD) and Liquids.

Location available after registration

Canada has established itself as a leading hub for pharmaceutical innovation, recognized for high-quality manufacturing, strong regulatory standards, and scientific excellence. In the field of contract development and manufacturing organizations (CDMOs), Canada stands out for its advanced facilities, skilled workforce, and robust quality systems. Partnering with CDMOs in Canada ensures access to reliable, high-quality pharmaceutical development and manufacturing services trusted by global markets.

Whether you are a biotech startup or an established pharmaceutical company seeking to outsource development, formulation, or production, Canadian CDMOs offer a strategic advantage for bringing drug products to market efficiently, safely, and in full regulatory compliance.

Why Choose CDMO Companies in Canada?

Canada combines a strong pharmaceutical heritage with a commitment to innovation and quality. Here’s why companies worldwide choose to work with CDMOs in Canada:

  • Regulatory Excellence: Canadian CDMOs comply with Health Canada regulations and align with global standards such as FDA and EMA, ensuring smooth international market access.
  • Precision Manufacturing: Known for robust quality systems, process control, and reliability in pharmaceutical manufacturing.
  • Advanced Technologies: Expertise in automation, continuous manufacturing, data integrity, and advanced analytical systems.
  • Highly Skilled Workforce: Canadian CDMOs employ experienced scientists, engineers, and quality professionals with deep expertise in regulated environments.

Key Services Offered by Canadian Contract Manufacturers

Leading CDMOs in Canada provide a comprehensive range of pharmaceutical services, including:

  • Drug Development: Pre-formulation, analytical development, formulation design, and process optimization
  • Clinical Manufacturing: GMP-compliant production of clinical trial materials
  • Commercial Manufacturing: Scalable production for domestic and international markets, including packaging and labeling
  • Sterile & Aseptic Manufacturing: Injectable drug products, vials, ampoules, and other sterile dosage forms
  • API Manufacturing: Small-molecule APIs and advanced intermediates under GMP conditions
  • Quality Assurance & Regulatory Support: Health Canada filings, global regulatory submissions, audits, and lifecycle management

Canadian CDMOs are particularly valued for projects requiring precision, strong quality systems, and reliable long-term manufacturing support.

Advantages of Partnering with CDMOs in Canada

Choosing a Canadian CDMO offers multiple strategic and operational advantages:

  • Uncompromising Quality: Canadian CDMOs maintain high standards to ensure consistent product quality and regulatory compliance.
  • Operational Reliability: Strong project management, risk mitigation, and supply continuity.
  • Technological Leadership: Advanced manufacturing, automation, and digitalization capabilities.
  • Global Regulatory Acceptance: Canadian-manufactured products are widely trusted by international regulatory authorities.

CDMO Companies in Canada

Some of the leading CDMOs in Canada include:

Experienced provider SV Chembiotech: CDMO in Canada providing pharmaceutical development and GMP manufacturing services. [See CDMO profile]

Related Information

Leading CDMO Companies in America

Leading CDMO Companies in USA

Let MAI CDMO Network Help You Find the Right Canadian Partner

At MAI CDMO, we connect pharmaceutical and biotech companies with the most suitable CDMOs in Canada. Whether you require support for drug development, contract manufacturing, API production, or sterile manufacturing, we simplify the process of identifying, qualifying, and engaging with the right Canadian CDMO to meet your project objectives.

Ready to explore your options? Contact us today and let us help you find a Canadian partner that meets your quality standards, timelines, and long-term growth goals.