Rentschler Biopharma SE
Rentschler Biopharma SE is a leading contract development and manufacturing organization (CDMO) dedicated to advancing biopharmaceuticals. Founded in 1872 and based in Laupheim, Germany, it is an independent family-owned company in its fifth generation, with over 1,400 employees across two locations. The company is committed to innovation, quality, and sustainability, aiming to drive progress in the biopharma industry and improve patient lives. The company adheres to a comprehensive code of conduct for suppliers emphasizing ethics, human rights, health and safety, environmental responsibility, and quality management, and maintains high standards of information security and data protection.
Industries
Nr. of Employees
large (251-1000)
Rentschler Biopharma SE
Laupheim, Baden-Wurttemberg, Germany, Europe
Services
Contract manufacturing of biopharmaceuticals under GMP, including sterile production, packaging and maintenance of production equipment.
Development and optimization of upstream and downstream processes for drug-substance scale-up and transfer to manufacturing.
Analytical method development, validation and routine quality-control testing for raw materials, intermediates and finished biopharmaceuticals.
Formulation design and development for biopharmaceutical drug products across different dosage forms.
Sterile filling and finishing of parenteral products, including packaging and labelling within GMP cleanrooms.
Program and project management services coordinating development, manufacturing and regulatory activities for client programs.
Contract manufacturing of biopharmaceuticals under GMP, including sterile production, packaging and maintenance of production equipment.
Development and optimization of upstream and downstream processes for drug-substance scale-up and transfer to manufacturing.
Analytical method development, validation and routine quality-control testing for raw materials, intermediates and finished biopharmaceuticals.
Formulation design and development for biopharmaceutical drug products across different dosage forms.
Sterile filling and finishing of parenteral products, including packaging and labelling within GMP cleanrooms.
Program and project management services coordinating development, manufacturing and regulatory activities for client programs.
Expertise Areas
- Biopharmaceutical cGMP manufacturing
- Process development and scale-up for biologics
- Analytical development and QC testing
- Formulation development for biopharmaceuticals
Key Technologies
- cGMP biomanufacturing platforms
- Aseptic filling and sterile packaging
- Bioprocessing (mammalian cell culture)
- Protein analytical assays and biochemical methods