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Coriolis Pharma Adds Analytical Ultracentrifugation for Release Testing to its Service Offerings

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Coriolis Pharma offers Analytical Ultracentrifugation (AUC) for biologics and virus-based drug products from early-stage development to post-market monitoring. Coriolis is now preparing for inspection by the competent surveillance authority for the confirmation to perform AUC services in compliance with GMP. The first clients have already started their projects.

MARTINSRIED-MUNICH, Germany, March 06, 2024, / Biotech Newswire / -- Coriolis Pharma, a globally operating service provider for drug product development, analytics and manufacturing support, proudly announces the introduction of Analytical Ultracentrifugation (AUC) under GMP. With the introduction of this method under GMP, Coriolis meets the increasing demand in the pharmaceutical and biotech industry and expands its existing portfolio of GMP methods for the development of high-quality drug products.

AUC has long been recognized as a powerful technique, even a gold standard, for the detailed study of macromolecules, including proteins, nucleic acids, viral vectors, and nanoparticles. Its ability to provide precise information on aggregation, molecule size, shape and interactions has made it indispensable in the field of biophysical characterization.

"Coriolis has been a world leading specialist for biopharmaceutical method development and testing by using AUC for almost a decade, featuring all available combinations of state-of-the-art AUC hard- and software," said Dr. Frank Schaubhut, Head of Operations at Coriolis Pharma. "We’re proud to take our expertise to the next quality level with introducing this service under GMP.”

From the early development to post-market monitoring: AUC has proven its versatility in the various phases of drug development: Formulation development, quality control, comparability studies or post-marketing surveillance. It is therefore an important addition to Coriolis' comprehensive range of phase-appropriate analytical services under GMP, which also includes method development and validation, compendial method verifiation, release testing, tech transfer support, and stability testing.

Coriolis' commitment to high-quality, innovation and scientific excellence has earned the trust of leading biopharmaceutical companies worldwide. By partnering with Coriolis for GMP analytical services, companies can accelerate their time to market, reduce costs and mitigate risks associated with product quality and regulatory compliance.

For more information about the AUC services of Coriolis, please visit https://www.coriolis-pharma.com/analytical-ultracentrifugation.


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About Coriolis Pharma
Coriolis Pharma is a globally operating contract research and development organization (CRDO) and one of the world leaders in formulation research and development of (bio)pharmaceutical drugs, including cell and gene therapy products and vaccines. It is the vision of Coriolis to revolutionize the development process of biopharmaceutical drugs by integrating innovative digital formulation approaches from drug development to commercial products. With its interdisciplinary team of highly skilled scientists and an expert scientific advisory board, Coriolis provides cutting-edge services and tailor-made solutions for its clients. Coriolis was founded in 2008 and currently employs more than 200 employees from over 36 nations around the world.



Coriolis Pharma Research GmbH
Bettina von Klitzing-Stückle
Scientific Marketing Manager
+49 (0) 89 4177 60 – 0
This email address is being protected from spambots. You need JavaScript enabled to view it.
Fraunhoferstr. 18b
82152 Martinsried-Munich


Keywords: Ultracentrifugation; Product Surveillance, Postmarketing; Quality Control; Drug Delivery Systems; Drug Development; Drug Compounding; Laboratories; Genetic Therapy; Biological Products; Pharmaceutical Preparations; Biotechnology; Germany; Coriolis Pharma; Analytical Ultracentrifugation (AUC); GMP (Good Manufacturing Practice); Martinsried-Munich; Drug product development; Biologics; Virus-based drug products; Post-market monitoring; Competent surveillance authority; Pharmaceutical industry; Biotech industry; Macromolecules; Proteins; Nucleic acids; Viral vectors; Nanoparticles; Biophysical characterization; Dr. Frank Schaubhut; Method development and testing; Formulation development; Quality control; Post-marketing surveillance; Phase-appropriate analytical services; Method validation; Stability testing; Regulatory compliance; Contract research and development organization (CRDO); Formulation research and development; Cell and gene therapy products; Vaccines; Digital formulation approaches

Published by Biotech Newswire

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