Complimentary Learning Level: Basic/Intermediate/Advanced Session Length: 1 hour The ISPE Process Analytical Technology (PAT) & Lifecycle Control Strategy (LCS) Steering Committee would like to engage the PAT & LCS...
Extended Learning Learning Level: Intermediate Session Length: 1.5 hours The Control Strategy becomes more and more important and many different control strategies must be in place to secure robust manufacturing...
Complimentary Learning Level: Intermediate Session Length: 1 hour As the volume of data within your operations continues to grow, it becomes increasingly difficult to integrate, manage and govern this data. For many...
Learning Level: Intermediate Session Length: 1.5 hours The pressure points of the COVID-19 pandemic have been an unprecedented challenge for the pharmaceutical industry and generated a global spotlight on supply...
Learning Level: Beginner/Intermediate Session Length: 1 hour Did you know that more than 80% of equipment failures in manufacturing are caused by human error or adverse operating conditions rather than time-based wear...
Learning Level: Beginner/Intermediate Session Length: 1 hour One of the major challenges for the industry today is designing digital “value creation” systems for sustainability. Sustainability requires balancing economic...
Learning Level: Beginner/Intermediate Session Length: 1 hour The pandemic was a unique time in our industry where there was a perfect storm of need, money, collaboration, and trial patients all available in abundance. ...
Complimentary Learning Level: Intermediate Session Length: 1.5 hour The ISPE Advancing Pharmaceutical Quality (APQ) program has been developed by industry representatives, for industry use, to advance the current state...
Extended Learning Learning Level: Basic/Intermediate Session Length: 1.5 hours Annex 1 , the section of the EU GMPs that regulates the manufacturing of sterile products, has been valid in the current version since 2009...
Extended Learning Learning Level: Advanced Session Length: 2 hours ICH Q12 , Technical and Regulatory Considerations for Pharmaceutical Product Lifecycle Management, is a transformative document that will shape global...
