In the news | 6th Sep 2022
How to avoid common pitfalls in the tech transfer process
Even the most well-established biotechnology companies can be challenged when it comes to implementing tech transfer successfully. Tech transfer processes bridge the gap between every stage of drug development for the transfer of information about development, manufacturing and quality assurance.
Read more on this topic in our article by Ken Forman, Senior Director of Product Strategy at IDBS, published in Labiotech.eu.
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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