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Leading CDMO Companies in Switzerland

Your Trusted Swiss Partners for Contract Manufacturing and Development

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Showing 11 facilities
SENN Chemicals | R&D and Kilo Lab | Dielsdorf, Switzerland
Switzerland

SENN Chemicals | R&D and Kilo Lab | Dielsdorf, Switzerland

Senn Chemicals

Swiss peptide and peptide intermediates R&D site with SPPS, LPPS, hybrid synthesis, kilo lab scale up, purification and analytics.

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

REGION: Europe

CATEGORY / PRODUCT: COSMETICS, CHEMICAL-SYNTHETIC, SERVICES, PARTICLE ENGINEERING

BATCH SIZE: Small

SENN Chemicals | Small Scale GMP Lab | Dielsdorf, Switzerland
Switzerland

SENN Chemicals | Small Scale GMP Lab | Dielsdorf, Switzerland

Senn Chemicals

Small scale GMP peptide and organic synthesis lab for clinical, niche and high value projects requiring flexible cGMP production.

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

REGION: Europe

CATEGORY / PRODUCT: CHEMICAL-SYNTHETIC, PARTICLE ENGINEERING

BATCH SIZE: Small

SENN Chemicals | GMP Production | Dielsdorf, Switzerland
Switzerland

SENN Chemicals | GMP Production | Dielsdorf, Switzerland

Senn Chemicals

Swiss cGMP production site for LPPS, SPPS and hybrid peptide manufacturing from pilot to early commercial scale.

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

REGION: Europe

BATCH SIZE: Large, Medium

CATEGORY / PRODUCT: CHEMICAL-SYNTHETIC, PARTICLE ENGINEERING

Aenova Group - Location Sisseln, Switzerland
Switzerland

Aenova Group - Location Sisseln, Switzerland

Aenova

Competence Center complex conventional solids.

REGION: Europe

MARKETS: FDA (USA), ANVISA (Brazil), Russian Health Authorities, MFDS (South Korea), Turkish Health Authorities

COMPLIANCE: FDA (cGMP), ISO, ANVISA (Brazil B-GMP), Roszdravnadzor (Russia GMP), World Health Organization (GMP / HACCP), MFDS/KFDA (Republic of Korea GMP)

BATCH SIZE: Large, Small, Medium

CATEGORY / PRODUCT: NUTRACEUTICALS, FDF / DRUG PRODUCTS

USE: Human

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

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

Aenova Group - Location Kirchberg, Switzerland
Switzerland

Aenova Group - Location Kirchberg, Switzerland

Aenova

Competence Center Soft gelatin capsules.

OEB (Occupational Exposure Banding): 5 / HPAPI (PDE < 10 µg/day), 4 / HPAPI (PDE = 10 - 100 µg/day), 2 (PDE = 1,000 - 10,000 µg/day), 3 (PDE = 100 - 1,000 µg/day), 1 / low-hazard (PDE > 10,000 µg/day)

MARKETS: EMA (EU), FDA (USA), Russian Health Authorities, SFDA (Saudi Arabia), MFDS (South Korea), Turkish Health Authorities, TGA (Australia)

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

REGION: Europe

COMPLIANCE: FDA (cGMP), ISO, Roszdravnadzor (Russia GMP), TGA (Australia GMP), TITCK (Turkish Health Authorities), SFDA (Saudi Food & Drug Authority), EMA (EU GMP), World Health Organization (GMP / HACCP), MFDS/KFDA (Republic of Korea GMP)

BATCH SIZE: Large, Small, Medium

CATEGORY / PRODUCT: COSMETICS, NUTRACEUTICALS, FDF / DRUG PRODUCTS

USE: Human, Veterinary

THERAPEUTIC AREAS OF EXPERTISE (ATC): (C) Cardiovascular system, (D) Dermatologicals, (H) Systemic hormonal preparations excl. sex hormones and insulins, (V06) Nutrients, (A) Digestive tract and metabolism, (G) Genito urinary system and sex hormones

Adragos Pharma | Jura
Switzerland

Adragos Pharma | Jura

Adragos Pharma

We specialize in aseptic manufacturing of lyophilized or liquid sterile (bio)pharmaceutical drug products through fill and finish.

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

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

REGION: Europe

COMPLIANCE: FDA (cGMP), EMA (EU GMP)

USE: Human

CONTROLLED SUBSTANCES: High potential for abuse & no medical use

BATCH SIZE: Small, Medium

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

CATEGORY / PRODUCT: FDF / DRUG PRODUCTS

Ophtapharm, a Sentiss Company
Switzerland

Ophtapharm, a Sentiss Company

Ophtapharm, a Sentiss Company

Ophtalmic and Otic - Solutions, suspensions, emulsions, ointments and gels - FDA Approved facility.

MARKETS: EMA (EU), FDA (USA)

REGION: Europe

COMPLIANCE: FDA (cGMP), ISO, EMA (EU GMP), World Health Organization (GMP / HACCP)

BATCH SIZE: Large, Small, Medium

USE: Human, Veterinary

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

CATEGORY / PRODUCT: FDF / DRUG PRODUCTS

Limited view

CHEMICAL-SYNTHETIC manufacturing site

MAI network supplier

Highly Potent APIs development and small-scale cGMP production including chromatography and lyophilization.

Location available after registration

Limited view

PARTICLE ENGINEERING manufacturing site

MAI network supplier

Development and cGMPmanufacturing of Highly Potent API including Antibody Drug Conjugates (ADC).

Location available after registration

Limited view

CHEMICAL-SYNTHETIC manufacturing site

MAI network supplier

Development and medium scale manufacturing.

Location available after registration

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HIPRA BIOTECH SERVICES | Aiguaviva
Spain

HIPRA BIOTECH SERVICES | Aiguaviva

HIPRA Biotech Services

End-to-end internal capabilities from cell line development to commercial manufacturing.

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

MARKETS: EMA (EU), PMDA (Japan), FDA (USA), Health Canada (Canada), ANVISA (Brazil), ISP (Chile), MSPAS (Guatemala), COFEPRIS (Mexico), DIGEMID (Peru), MHRA (UK), ANMAT (Argentina), INVIMA (Colombia)

COMPLIANCE: DIGEMID, FDA (cGMP), ISO, PMDA/MHLW (Japan GMP), ANVISA (Brazil B-GMP), MSPAS, COFEPRIS, INVIMA, ISP (Chile BPM), ANMAT (Argentina nueva GMP), EMA (EU GMP), Health Canada (Canada GMP), World Health Organization (GMP / HACCP), MHRA (UK GMP)

BSL (Biological Safety Level): 1, 2

USE: Human

BATCH SIZE: Large, Small, Medium

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

REGION: Europe

CATEGORY / PRODUCT: BIOLOGICS

Adare Pharma | EU
Italy

Adare Pharma | EU

Adare Pharma Solutions

Global CDMO offering turnkey product development through commercial manufacturing expertise, focused on oral dosage forms.

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

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

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

USE: Human, Veterinary

BATCH SIZE: Large, Small, Medium

THERAPEUTIC AREAS OF EXPERTISE (ATC): (N) Nervous system, (J) Antiinfectives for systemic use, (V01) Allergens, (R) Respiratory system, (M) Musculoskeletal system, (C) Cardiovascular system, (A) Digestive tract and metabolism

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

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

REGION: Europe

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Switzerland has earned its place as a global pharmaceutical powerhouse, renowned for precision, quality, and innovation. When it comes to contract development and manufacturing organizations (CDMOs), the country stands out for its advanced infrastructure, regulatory excellence, and experienced workforce. Partnering with CDMOs in Switzerland ensures access to some of the most reliable and technologically advanced manufacturing capabilities in Europe and beyond.

Whether you're a biotech startup or a large pharmaceutical brand looking to outsource development, formulation, or production, Swiss CDMOs offer a strategic advantage in bringing your products to market efficiently and compliantly.

Why Choose CDMO Companies in Switzerland?

Switzerland offers an unmatched combination of pharmaceutical heritage, regulatory excellence, and technical know-how. Here's why companies worldwide choose to work with CDMOs in Switzerland:

Ensuring global compliance through Regulatory Expertise: Swiss CDMOs operate under strict compliance with EMA, FDA, and Swissmedic guidelines, ensuring high global standards.

Fostering biopharmaceutical advancements as an Innovation Hub: Home to pharmaceutical giants and R&D centers, Switzerland fosters constant innovation and advanced capabilities in biologics, sterile manufacturing, and high-potency compounds.

Optimizing European supply networks via a Strategic Location: Situated in the heart of Europe, Swiss CDMOs offer efficient logistics for global supply chains.

Leveraging technical excellence from a Skilled Workforce: With a deep pool of scientific and technical talent, Swiss CDMOs ensure your project is in capable hands from development through commercialization.

Key Services Offered by Swiss Contract Manufacturers

Most of the CDMOs in Switzerland provide a wide range of end-to-end pharmaceutical services, including:

Optimizing formulation techniques in Drug Development: Pre-formulation, analytical development, process optimization.

Supplying clinical trial phases via Clinical Manufacturing: Small-batch production under GMP conditions for clinical trials.

Scaling up commercial production in Commercial Manufacturing: Large-scale production for global markets, including packaging and labeling.

Maintaining high sterility standards in Sterile & Aseptic Manufacturing: Injectable, ophthalmic, and other sterile dosage forms.

Developing cell line processes in Biologics & Biosimilars: Cell line development, upstream/downstream processing.

Managing high-containment protocols for High Potency & Controlled Substances: Specialized containment and safety infrastructure.

Navigating global audit requirements through Quality Assurance & Regulatory Support: Assistance with filings and audits.

Swiss CDMOs often specialize in niche or complex areas, such as orphan drugs, nanoparticle delivery systems, and high-barrier generics.

Advantages of Partnering with CDMOs in Switzerland

Choosing a Swiss CDMO can offer numerous strategic and operational benefits:

Setting global pharmaceutical standards with Quality Without Compromise: Swiss precision is more than a cliché—it’s a pharmaceutical standard.

Reducing time to market through Accelerated Timelines: Streamlined regulatory pathways and efficient project management help reduce time to market.

Building long-term business relationships through Trust & Transparency: Swiss business culture emphasizes long-term partnerships and ethical practices.

Integrating modern digital infrastructure for a Technological Edge: Cutting-edge facilities and digital manufacturing integration deliver operational excellence.

Simplifying international market access via Global Compliance: Seamless adherence to global regulatory requirements, simplifying market access.

CDMO Companies in Switzerland

Some of the top CDMOs in Switzerland include:

Aenova: Competence Center for soft gelatin capsules in Switzerland. [See CDMO profile]

Ophtapharm, a Sentiss Company: CDMO in Switzerland for ophthalmic and otic solutions, suspensions, emulsions, ointments, and gels. [See CDMO profile]

APR LAB: Contract Service Unit of a Swiss biopharmaceutical company focused on identifying, developing, and marketing innovative treatments for rare and ultra-rare diseases worldwide. [See CDMO profile]

Adragos Pharma: Specializing in aseptic manufacturing of lyophilized and liquid sterile (bio)pharmaceutical drug products through fill-and-finish processes. [See CDMO profile]

CARBOGEN AMCIS: Expert in the development and cGMP production of highly potent APIs at small and medium scale, including chromatography and lyophilization capabilities. [See CDMO profile]

Related Information

Leading CDMO Companies in Europe

Leading CDMO Companies in Germany

Leading CDMO Companies in Italy

Leading CDMO Companies in France

Let MAI CDMO Network Help You Find the Right Swiss Partner

At MAI CDMO, we specialize in connecting pharmaceutical and biotech companies with the most suitable CDMOs in Switzerland. Whether you're seeking a partner for complex biologic manufacturing or early-phase development support, we streamline the process of finding, qualifying, and engaging with the right Swiss CDMO for your needs.

Contact us today and let’s help you find a Swiss partner that meets your timeline, quality standards, and growth goals.