
Adragos Pharma
End-to-end CDMO partner for small molecules and biologics across seven global facilities.
Global CDMO Headquartered in Munich, Germany.
Modalities
Development & manufacturing
Structured CDMO capabilities from verified public sources.
Manufacturing (M)
Biologics / bioreactor infrastructure
- Expression systems
- Mammalian
Synthetic chemistry infrastructure
- Capabilities
- HPAPIDEA licensed
Fill-finish formats
Regulatory clearances
Services
- Formulation Development
- CMC Analytical Development
- Process Development
- Stability Testing & Storage
- Quality Control Testing
- CMC Regulatory Submission Support
- HPAPI Manufacturing (High-Potency)
- Lyophilization (Freeze Drying)
- Prefilled Syringe (PFS) Filling
- Vial Filling
- Sterile Fill-Finish & Aseptic Manufacturing
- Oral Solid Dosage Manufacturing
- Topical & Semi-Solid Manufacturing
- Cold-Chain Storage & Logistics
- Secondary Packaging & Labeling
- Technology Transfer
- Monoclonal Antibody (mAb) Manufacturing
Indications
About this organization
Adragos Pharma is a Contract Development and Manufacturing Organisation (CDMO) with a global presence spanning Europe, Japan, and North America. The company operates an integrated network of seven strategically located facilities (Athens, Halden, Jura, Kawagoe, Livron, Leipzig, and Maisons-Alfort) dedicated to delivering end-to-end pharmaceutical development and manufacturing services.
Core Capabilities
Drug Development & Formulation
- Formulation development across multiple dosage forms
- Analytical development and method development
- Clinical development support
- Expertise in HPAPI (highly potent active pharmaceutical ingredients)
- Process development and optimization
Manufacturing Services
- Sterile Liquids: vials, ampoules, IV bags, prefilled syringes
- Non-Sterile Liquids: oral solutions, oral drops, suspensions, emulsions, disinfection products
- Semi-Solids: creams, ointments, gels, healing pastes
- Oral Solids: suppositories and other solid dosage forms
- Aseptic filling and lyophilization capabilities
- Commercial manufacturing at scale
Clinical & Regulatory Support
- Preclinical material preparation
- Clinical supply manufacturing with GMP compliance
- Regulatory affairs and CMC support
- Supply chain planning and cold chain management
- Drug stability testing
- Visual inspection and pharmaceutical packaging
- Out-licensing services
Regulatory Compliance
Adragos Pharma adheres to standards set by the FDA (U.S. Food and Drug Administration), EMA (European Medicines Agency), and PMDA (Pharmaceuticals and Medical Devices Agency in Japan). The company implements rigorous quality control and assurance measures throughout development and manufacturing to ensure global market compliance.
Differentiation
The company emphasizes a customer-centric approach with dedicated project managers, flexible timelines, and seamless coordination across its global network. Client testimonials highlight technical expertise in complex formulations, transparency in quotations, and ability to advance projects from concept to registered marketable product on budget and on time.
Locations
Headquarters
Munich · Bavaria · Germany
Development & Manufacturing
Athens · Attica · Greece
Manufacturing
Halden · Østfold · Norway
Manufacturing
Jura · Bourgogne-Franche-Comté · France
Manufacturing
Kawagoe · Saitama · Japan
Manufacturing
Livron · Auvergne-Rhône-Alpes · France
Manufacturing
Leipzig · Saxony · Germany
Manufacturing
Maisons-Alfort · Île-de-France · France
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