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.
As with all aspects of our life sciences industry, understanding how we can best meet the needs of patients with the timely delivery of life saving and sustaining products is of paramount concern. During the years since the global pandemic, the expectations and pressures on the pharmaceutical industry with respect to development, speed to market, quality and sustainability have increased...
At the 2024 ISPE Europe Annual Conference, held in Lisbon, Portugal, 16-18 April, Richard L. Friedman, MS, Deputy Director of the US Food and Drug Administration’s (US FDA) Office of Manufacturing Quality, in...
Insight from Austria’s Regulatory Authority Representative
At the 2024 ISPE Aseptic Conference, held March 12-13 in Vienna, Austria, Christina Meissner, a European Union Good Manufacturing Practice (GMP) inspector at the Austrian Agency for Health and Food Safety since 2013, and Chair of the PIC/S Drafting Group on Annex 2A and 2B, published in May 2021, offered a presentation titled...