INTERPHEX Cleaning Validation Considerations for Continuous Manufacturing Processes
October 15th, 2015 – 4:00-5:00 PM
Steris Life Sciences Manager of Technical Services, Paul Lopolito, and Technical Services Specialist, Elizabeth Rivera, will be presenting continuous manufacturing focuses on streamlining production while minimizing the process footprint and waste from non-value activities. To ensure cGMP compliance cleaning is required on some frequency between batches of the same product and when switching between different products. The presentation will share cleaning options for light and heavy cleaning activities of continuous process equipment and calculating acceptance limits for non-uniform residues. The presentation will also discuss critical process parameters for cleaning and ways to drive out waste while ensuring compliance.
Click here for additional information.