The drive to meet sustainability objectives while increasing efficiencies in the QC laboratory can sometimes seem overwhelming.
This presentation will highlight options to future-proof laboratory operations for endotoxin and pyrogen testing through sustainable methods, automation, and digitalization solutions. Furthermore, current regulatory requirements and impacts for sustainable endotoxin and pyrogen testing will be explored.
The advantages to be gained from implementation of solutions during manufacturing and batch release of pharmaceutical products will be discussed.
- Spotlight on SDGs and how they may impact QC testing
- Regulatory news for moving towards sustainable endotoxin and pyrogen testing
- Advantages gained from implementing automated and digitalized solutions
Presenters:
Katrin Pauls - Market Development and Scientific Affairs Manager, Lonza Bioscience Solutions
Sinéad Cowman - Global Business Development & Marketing Manager, Lonza Bioscience Informatics
Moderator:
Janet Yancey-Wrona - Director Marketing Testing, Lonza Bioscience Solutions
Who should attend?
Sponsors, pharma, biotech and medical device manufacturers, microbiology program/project managers, subject matter experts, QC/QA supervisors, managers and lab personnel.
