Thursday, 20 June | 0700–1800
Friday, 21 June | 0700–1600
Hear about lessons learned for bioprocess validation and the assurance of reproduciblebioprocessing from the review of biosimilar applications
In this two-part workshop, you will select from a range of hot topics and break out into groups to formulate problem statements, discuss these issues, and share experiences
Make the most of your professional development by attending in-depth training on 24–26 June in four critical areas of pharma manufacturing.
We welcome your feedback throughout the year on ISPE's continuing education events. A survey will be emailed to all attendees at the close of the conference. Thank you for providing your feedback and ideas for future topics.
Follow the official hashtag of the 2019 ISPE Process Validation Workshop #ISPEPV to stay up to date on what is going on throughout the event, and use it to share your own experiences on social media.
Stability sampling and testing are key to ensuring that products maintain safety, identity, strength, purity, and quality throughout their claimed shelf life. It is also a regulatory requirement per ICH Q5. However, storing product samples in different environmental conditions, testing those samples for three to five years (or more) after initial manufacture, and properly analyzing and...
ISPE hosted more than 450 attendees in person and virtually for the 2024 ISPE Aseptic Conference in Vienna, Austria. Keynotes and education sessions provided a comprehensive overview of key topics and trends...
Biopharmaceutical facility design is a critical aspect of the industry. Overall cost pressures in the global health system, regional requirements to deploy manufacturing rather than centralize manufacturing in one location, technology enhancements in cell biology and format, flexibility to accommodate multi-product campaigns with different production schedules, and speed-to-market are among...