BIO International Convention 2025German Exhibitors Coriolis Pharma Research GmbH

Coriolis Pharma Research GmbH

www.coriolis-pharma.com

About us

Coriolis Pharma is a global contract research and development organization (CRDO) and the premier partner for the development of liquid and lyophilized drug products, analytical services, and manufacturing services across a broad range of therapeutic modalities, including biologics, gene and cell therapies and vaccines.

Our expert scientists design and execute platform and custom services to accelerate and derisk your programme right from the start and throughout the entire product lifecycle.

Coriolis Pharma is headquartered in Martinsried, Germany, with representatives around the world and an additional office in the USA.

Drug Development Services

Analytical Services under R&D and GMP

Manufacturing Services

Formulation Development

Particle Characterization

Particle Identification

Analytical Ultracentrifugation

Lyophilization

Stability and Release Testing

Address

Coriolis Pharma Research GmbH
Fraunhoferstraße 18b
82152 Martinsried
Germany

E-mail: business.development@coriolis-pharma.com
Phone:  +49 89 417760-0
Internet: www.coriolis-pharma.com
Coriolis Pharma US Inc.
455 E Eisenhower Pkwy
Suite 300, #1130
MI 48108 Ann Arbor
United States

E-mail: business.development@coriolis-pharma.com
Phone:  +1 256 400-4491
Internet: www.coriolis-pharma.com

Contact person:

Dr. Evelyn Eggenstein
Director Commercial Operations US
E-mail: evelyn.eggenstein@coriolis-pharma.com
Phone: +1 248 679 6167

Johannes Clemens
Chief Commercial Officer
E-mail: johannes.clemens@coriolis-pharma.com
Phone: +49 89 41 77 60 -0

Products & Services

Biotechnology
Laboratories
Medicine / Pharmaceutics
Nanotech & Products

Development Services

  • Developability assessment

  • Pre-formulation screening

  • Formulation development, optimisation and robustness

  • Stability studies

  • Primary packaging and container closure selection

  • Forced degradation studies

  • Clinical/commercial in-use and compatibility studies

  • Life cycle management and reformulation

Analytical Services under R&D and GMP

  • Method development, qualification, and transfer

  • Phase-appropriate method validation

  • Compendial method verification

  • Release testing / Tech transfer support

  • Stability studies

  • Fast track analytics

  • Particle characterisation

  • Particle identification

Manufacturing Services

  • Tox study manufacturing

  • Filing of reference material

  • Lead lot stability material

  • Lyophilization process development, optimisation, transfer and scale-up

  • Comparability, pump, headspace & CCIT studies

  • Process development

  • Manufacturing troubleshooting

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