Solupharm Pharmaceutical Products GmbH
Solupharm is a family-owned company specializing in high-quality contract manufacturing of sterile preparations in glass ampoules and vials. Since 1974, it has been a reliable partner for national and international customers, operating one of Europe's most modern production facilities in Melsungen, Germany. The company emphasizes quality, innovation, and responsibility in the production of parenteral medicines. With nearly 50 years of experience, state-of-the-art technology, and a strong commitment to GMP standards, Solupharm offers comprehensive services including quality control, sterile production, packaging, quality assurance, warehousing, and technical development. The company is committed to continuous growth, aiming to double its capacity by 2029, and maintains a strong focus on quality, safety, and customer satisfaction.
Industries
Nr. of Employees
medium (51-250)
Solupharm Pharmaceutical Products GmbH
Products
Water for injection and electrolyte solutions
Sterile aqueous solutions intended for parenteral use produced via aseptic or terminal processes and released after validated QC testing.
Sterile medicinal liquid products (analgesics, anaesthetics, herbal/homeopathic formulations)
Aseptically manufactured or terminally sterilised finished medicinal products in ampoules and vials for therapeutic use, produced in multiple container sizes.
Water for injection and electrolyte solutions
Sterile aqueous solutions intended for parenteral use produced via aseptic or terminal processes and released after validated QC testing.
Sterile medicinal liquid products (analgesics, anaesthetics, herbal/homeopathic formulations)
Aseptically manufactured or terminally sterilised finished medicinal products in ampoules and vials for therapeutic use, produced in multiple container sizes.
Services
End-to-end manufacture of sterile liquid medicinal products including aseptic filling and terminal sterilisation into glass ampoules and glass vials across multiple container sizes, with GMP-compliant production and batch release testing.
Chemical-physical, microbiological and chromatographic testing for raw materials, in-process samples and final product release using validated methods and full documentation.
Automated and manual packaging workflows including 100% visual inspection, high-precision labelling, customised packaging formats and serialization/aggregation to meet regulatory track-and-trace requirements.
Storage and handling for packaging materials, raw materials, intermediates and finished goods including automated storage systems and controlled-temperature storage areas for regulated substances.
Technical services covering preventive maintenance, utilities and pharmaceutical water management, equipment procurement/modification, qualification and validation to maintain regulatory compliance and machine availability.
Development, deployment and operation of internal business applications and hosted services, including management of hosting providers, data processing contracts, web analytics governance and compliance with data protection regulations and frameworks.
End-to-end manufacture of sterile liquid medicinal products including aseptic filling and terminal sterilisation into glass ampoules and glass vials across multiple container sizes, with GMP-compliant production and batch release testing.
Chemical-physical, microbiological and chromatographic testing for raw materials, in-process samples and final product release using validated methods and full documentation.
Automated and manual packaging workflows including 100% visual inspection, high-precision labelling, customised packaging formats and serialization/aggregation to meet regulatory track-and-trace requirements.
Storage and handling for packaging materials, raw materials, intermediates and finished goods including automated storage systems and controlled-temperature storage areas for regulated substances.
Technical services covering preventive maintenance, utilities and pharmaceutical water management, equipment procurement/modification, qualification and validation to maintain regulatory compliance and machine availability.
Development, deployment and operation of internal business applications and hosted services, including management of hosting providers, data processing contracts, web analytics governance and compliance with data protection regulations and frameworks.
Expertise Areas
- Contract sterile parenteral manufacturing (aseptic filling and terminal sterilisation)
- Analytical testing and quality control for parenteral products
- Packaging, labelling, serialization and track-and-trace for finished medicinal containers
- GMP quality assurance and regulatory inspection readiness
Key Technologies
- Aseptic filling technology
- Terminal sterilisation processes
- High-performance liquid chromatography (HPLC)
- Gas chromatography (GC)
News & Updates
Company Expansion and Capacity Increase
Solupharm plans to double its capacity by 2029, increasing annual filling capacity to 300 million ampoules and 40 million vials, supported by a new modern building.
Company History and Development
Emerging from the family-run Aesculap pharmacy, Solupharm has grown into one of Europe's leading contract manufacturers for parenterals, with a focus on quality, innovation, and responsibility.
Quality and Responsibility
The company emphasizes high standards, GMP compliance, and a motivated team to ensure the safety and efficacy of its products.
ISO Certification 2022
Achieved ISO certification for quality management systems, demonstrating commitment to quality standards.
GMP Compliance Recognition 2023
Received recognition for GMP compliance during international inspections, affirming high-quality manufacturing processes.
Company Expansion and Capacity Increase
Solupharm plans to double its capacity by 2029, increasing annual filling capacity to 300 million ampoules and 40 million vials, supported by a new modern building.
Company History and Development
Emerging from the family-run Aesculap pharmacy, Solupharm has grown into one of Europe's leading contract manufacturers for parenterals, with a focus on quality, innovation, and responsibility.
Quality and Responsibility
The company emphasizes high standards, GMP compliance, and a motivated team to ensure the safety and efficacy of its products.
ISO Certification 2022
Achieved ISO certification for quality management systems, demonstrating commitment to quality standards.
GMP Compliance Recognition 2023
Received recognition for GMP compliance during international inspections, affirming high-quality manufacturing processes.