In the news | 1st Feb 2022
What's in Store for 2022? Our Experts Weigh in
Around this time last year, the first COVID-19 vaccines were authorized for emergency use by organizations such as the FDA, the EMA, the MHRA and many more internationally. A year before that, COVID-19 had not yet been declared a pandemic. It goes to show how much can change in this industry, as well as how important this sector is. With what we know – having adapted constantly since March 2020 and having also experienced uncertainty as new variants are discovered – predictions from industry experts for 2022 are important and illuminating.
Hear from experts, including Alberto Pascual, in this article, published in Drug Discovery World.
Putting Your CMC Ontology to Work | Pistoia Alliance 2026
Join IDBS at the Pistoia Alliance conference as Ken Forman explores how organizations can transform a documented CMC ontology into a GxP-qualified operational framework. Learn how linking ontology to experimental data enables structured, submission-ready information, improving data exchange, regulatory compliance, and the efficiency of CMC processes.
CMC regulatory submissions: Why knowledge continuity matters
Biopharma organizations have invested heavily in managing CMC data, yet many continue to face a less visible challenge: preserving the knowledge behind critical development decisions. As products progress through development and teams evolve, maintaining scientific context can become just as important as maintaining the underlying data.
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