Cleanroom Conceptual Design Paradigm: Converting Spaces For GMP Operations Part 2

The conceptual design phase is critical when adapting non-traditional facilities into cGMP-compliant cleanrooms. Proper integration of process architecture and mechanical systems at this stage is essential for mitigating risk and ensuring the facility meets all operational requirements. This session focuses on the technical details of that integration. Our speakers explain the foundational design principles needed to implement cGMPs and satisfy regulatory bodies. They cover design strategies applicable to vaccine production, fill-finish, OSD, and cell and gene therapy facilities.

Watch now to learn how to apply these conceptual design strategies to your projects.