Topic: Quality

21 September 2026

Case study: Scale siRNA manufacturing efficiently via a fragment and enzymatic ligation approach

As demand for siRNA therapeutics continues to grow, manufacturers face increasing pressure to deliver larger quantities of drug…

03 August 2026

Case study: Verification of SAX method selectivity using 2D-LC-MS for peak purity assessment of oligonucleotide APIs

Accurate analytical characterization is essential throughout oligonucleotide development, supporting impurity profiling, stability assessment, and ultimately the delivery of…

20 July 2026

API contract manufacturing: Process, benefits, and partner selection

Manufacturing active pharmaceutical ingredients (APIs) is a complex undertaking that requires specialized process knowledge, advanced manufacturing capabilities, and…

15 April 2026

A Step-By-Step Guide to Analytical Method Development and Validation

Analytical method development and validation are essential foundations of pharmaceutical and biotechnology workflows. These processes ensure that analytical…

14 April 2026
07 October 2025

Webinar How to assess and reduce Nitrosamine Contamination Risks in Peptide APIs

Recent years have seen drug recalls based on nitrosamine drug substance related impurities (NDSRIs), with medical agencies advising…

18 July 2025

Expert Round – Outsourcing in Pharma 2025

The expert panel discussion focused on evolving trends in the pharmaceutical industry, particularly the growing importance of external…