Future-Proofing The Material Transfer Process In Your Facility With Automated Bio-Decontamination

Ensuring the safe transfer of sensitive living materials into sterile Grade A/ISO 5 environments is a major hurdle for cell and gene therapy manufacturers. How do you prevent contamination without damaging the very materials you're working with during bio-decontamination? Achieving consistency and quality in your material transfer process is paramount for both patient safety and regulatory compliance. This webinar explores how integrating modern automated bio-decontamination systems with established manual disinfection protocols can effectively mitigate risks and future-proof your facility.

Learn pragmatic strategies to enhance your material transfer program for current and future needs. Click below to watch the full on-demand webinar.