Biodecontamination plays a critical role in ensuring aseptic conditions within pharmaceutical manufacturing environments. Selecting and integrating the right technology becomes essential for compliance as well as for process reliability, efficiency, and validation feasibility, for example the use of dry fog or VHP.
Our experts Dr. Marina Gole, Senior Scientist in the GMP Compliance team, and James Drinkwater, Head of GMP Compliance, have combined their knowledge and are offering a webinar on the topic of “Scientific Insights into Vaporized Hydrogen Peroxide (VHP) Biodecontamination and managing BI quality variances”.
The Webinar on September 24, 2025 is organized in cooperation with Körber BA Pharma and Pharmaceutical Online.
More information and registration you can find on the event-site of the webinar.
