Analytical Procedure Development for Novel Peptides: From Column Screening to GMP Releases

In the current pharmaceutical landscape, therapeutic peptides are on the rise. To ensure the large-scale production of peptides in the highest quality, Bachem implements a holistic analytical control strategy. Beginning with product-specific understanding of e.g. related impurities and aggregation behavior, state-of-the-art chromatographic detection methods are developed and validated. This approach alongside the process development enables that stringent product specifications in line with current regulatory demands are continuously met.

About the Speaker

Priska Frei, Ph.D.

Scientist QC

Priska Frei studied Pharmaceutical Sciences. In 2018, she received her Ph.D. from the University of Basel (Switzerland) for her work on therapeutically promising carbohydrates. She then proceeded to work at the Institute of Legal Medicine of Basel-Stadt, where she developed analytical methods for the detection of psychoactive substances in biological matrices. In the beginning of 2022, she joined Bachem as scientist in the analytical development. Her responsibilities focus on chromatographic method development for peptide NCE projects.