Application Note |
By Ralph Melfi,AES Clean Technology, Inc.
Your future cleanroom is a critical asset, not just another construction project. The investment you make in the cleanroom facility is significant and it should perform for years to come. Learn the relative strengths and weaknesses of various cleanroom construction methodologies that are being implemented within the marketplace.
Compliance with quality control (QC) standards is a basic requirement for products manufactured under good manufacturing practices (GMP) conditions. In this post we will explore the main compendial QC tests that ensure cell and gene therapies are safe for use in patients, as well as important considerations for integrating QC testing into the manufacturing process.
Single-use technology (SUT) has transformed biopharmaceutical development and manufacturing. While the benefits of SUT in bioprocessing are clear, the pathways to successfully apply SUT continue to rapidly evolve. The ability to seamlessly combine multiple components and systems is critical.
Planning your flow cytometry experiment can be time-consuming. With this in mind, this new poster aims to help you plan your experiment by going through the key steps you need to consider before you start.