Bio-Europe 2024German Exhibitors Coriolis Pharma Research GmbH

Coriolis Pharma Research GmbH

Booth number: 180-06
www.coriolis-pharma.com

About us

Coriolis Pharma is a global contract research and development organization (CRDO) supporting the development of liquid and lyophilized drug products. We are committed to advancing biologics innovation through our exceptional drug product development, analytical, and manufacturing services. With a legacy of scientific excellence and a dedication to innovation, we have become the global partner for drug product innovators, supporting every phase of drug development from R&D to GMP. Our collaborative approach and profound scientific expertise establish us as a trusted partner from early-stage formulation to commercial manufacturing.

At Coriolis, we have a unique analytical portfolio of more than 200 different techniques - all performed in-house - to provide orthogonal and meaningful data. The in-house lyophilization development center enables our scientists to achieve time-saving and robust lyophilization cycles at laboratory, pilot and production scale. Dedicated GMP facilities allow us to perform lot release analysis and generate data to support regulatory submissions, as well as allow for customized "enhanced R&D" level studies.

Analytical Lab at Coriolis

Analytical Ultracentrifugation

Coriolis Lab

Development Services

Tox Batch Filling

Development Services for Liquids and Lyophilized Drug Products

Particle Characterization

Particle Identification

Address

Coriolis Pharma Research GmbH
Fraunhoferstraße 18b
82152 Martinsried/Munich
Germany

E-mail: business.development@coriolis-pharma.com
Phone:  +49 89 41 77600
Internet: www.coriolis-pharma.com

Contact person:

Dr. Daniel Weinbuch
E-mail: daniel.weinbuch@coriolis-pharma.com
Phone: +49 89 417760-149

Michel Croes
Business Development Manager
E-mail: michel.croes@coriolis-pharma.com
Phone: +49 89 417760-147

Products & Services

Biotechnology
Laboratories
Medicine/Pharmaceutics

We provide drug procuct development, analytical and manufacturing services from early development to commercialization

  • Developability assessment

  • Preformulation development

  • Forced degradation studies

  • Formulation development and optimization

  • Formulation robustness

  • Stability studies

  • Clinical in-use studies

  • Container closure selection

  • Tox study manufacturing

  • Lyophilization process development and optimization

  • Lyophilization process scale-up and transfer

  • Process characterization

  • Troubleshooting

  • Method development

  • PPQ/Phase-appropriate method validation

  • Compendial method verification

  • Release testing / Tech transfer support

  • Particle identification & characterization

  • Fast-track analytics

Drug Product Development

Development Services from Early Development to Commercialization

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Analytical Services

Analytical support for liquids and lyophilized drug products under R&D and GMP and up to biosafety level 2

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Manufacturing Services

Non-GMP manufacturing for liquids and lyophilized drug products

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