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TIDES Europe: Oligonucleotide and Peptide Therapeutics
11-13 November 2025
Congress Center BaselBasel, Switzerland

Dr. Daniela Fischer, Ph.D.
Associate Director Regulatory Affairs CMC at Novartis Pharmaceutical Manufacturing
Speaker

Profile

Daniela Fischer has worked in the pharmaceutical industry for over 15 years, mainly in analytical development and Regulatory CMC. She began her career at Carbogen Amcis AG and then worked at Bruker Biospin AG and Sandoz GmbH in analytical development before moving to Regulatory CMC at Sandoz GmbH and later Novartis, where she covered small molecules (generics), biosimilars and since 2021 synthetic oligonucleotides. She holds a Ph.D. in organic chemistry from the University of Regensburg, Germany.

Agenda Sessions

  • Regulatory CMC Insights on Post-approval Changes for a siRNA Oligonucleotide

    16:15