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DTSTART;TZID=America/Los_Angeles:20260902T110000
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DTSTAMP:20260812T085616Z
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UID:10924-1788346800-1788350400@thebiocalendar.com
SUMMARY:AI-Readiness in a Regulated World: A Practical Playbook for Life Sciences
DESCRIPTION:In this practical session\, Jake Walton\, VP of Quality & Compliance at MasterControl\, will share a candid look at how MasterControl approached AI the right way from the start—building human-in-the-loop architecture as a non-negotiable design principle\, aligning every capability to 21 CFR Part 11\, EU MDR\, GDPR\, HIPAA\, and other applicable standards\, and going all the way through ISO 42001 certification for Artificial Intelligence Management Systems.
URL:https://thebiocalendar.com/event/ai-readiness-in-a-regulated-world-a-practical-playbook-for-life-sciences/
LOCATION:Online webinar
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/png:https://thebiocalendar.com/wp-content/uploads/2026/08/09-02-26-MasterControl-LinkedIn-1280x720-1.png
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DTSTART;TZID=America/Los_Angeles:20260902T110000
DTEND;TZID=America/Los_Angeles:20260902T120000
DTSTAMP:20260812T085636Z
CREATED:20260805T160301Z
LAST-MODIFIED:20260812T085636Z
UID:10929-1788346800-1788350400@thebiocalendar.com
SUMMARY:A CCS is a purpose-built machine\, not a black box: Understand the workings
DESCRIPTION:A contamination control strategy (CCS) is usually treated as a document with sixteen elements assembled\, signed\, and shelved. This webinar offers a new perspective of a CCS as a machine that is not so complex that it cannot be analyzed component by component.
URL:https://thebiocalendar.com/event/a-ccs-is-a-purpose-built-machine-not-a-black-box-understand-the-workings-2/
LOCATION:Online webinar
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/png:https://thebiocalendar.com/wp-content/uploads/2026/08/09-02-25-CAI-LinkedIn-1280x720-1.png
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DTSTART;TZID=America/Los_Angeles:20260902T110000
DTEND;TZID=America/Los_Angeles:20260902T120000
DTSTAMP:20260812T085657Z
CREATED:20260805T181245Z
LAST-MODIFIED:20260812T085657Z
UID:10936-1788346800-1788350400@thebiocalendar.com
SUMMARY:Enabling the full potential of process chromatography
DESCRIPTION:Successfully scaling a purification process from development to GMP manufacturing requires maintaining process performance while minimizing variability. However\, scale-up often introduces challenges that can impact productivity\, recovery\, and overall process efficiency. To mitigate risk\, manufacturers frequently apply conservative safety factors during scale-up—resulting in lower resin utilization\, increased buffer consumption\, longer process times\, and reduced overall productivity. \nWhat if you could maintain the same critical process parameters (CPPs) and critical quality attributes (CQAs) from bench scale through commercial manufacturing with greater confidence and control? \nJoin Repligen for an in-depth discussion on how advanced process control and real-time analytics can help close the gap between process development and manufacturing performance. \nThis webinar will explore key considerations for implementing real-time monitoring and control strategies in chromatography processes. Industry experts will discuss the capabilities of the KRM® chromatography platform and the integration of FlowVPX® Process Analytical Technology (PAT) for in-line product concentration measurement. \nAttendees will learn how these technologies can be applied to support process characterization\, monitor purification performance\, and generate data that may inform scale-up and manufacturing decisions while maintaining focus on critical quality attributes. \nWhat You’ll Learn: \nWhy purification processes often lose efficiency during scale-up\nHow improved process accuracy and precision can increase yield and productivity\nBest practices for maintaining CPPs and CQAs from development through GMP manufacturing\nHow the KRM® platform supports advanced chromatography process control\nHow integrated FlowVPX® PAT enables real-time concentration monitoring and process optimization\nStrategies to improve resin utilization\, reduce buffer consumption\, and maximize recovery \nWho Should Attend? \nProcess Development Scientists\nDownstream Process Engineers\nManufacturing Scientists\nMSAT Professionals\nBiologics and Cell & Gene Therapy Professionals\nPurification and Chromatography Specialists \nRegister Today \nDiscover how real-time process analytics and intelligent chromatography control can help you achieve higher yields\, greater process consistency\, improved resin utilization\, and increased manufacturing productivity—without compromising product quality.
URL:https://thebiocalendar.com/event/enabling-the-full-potential-of-process-chromatography/
LOCATION:Online webinar
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/png:https://thebiocalendar.com/wp-content/uploads/2026/08/09-02-26-Repligen-Reg-1920x250-1.png
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