Data Integrity Considerations When
Selecting Your Endotoxin Testing Solution
Selecting Your Endotoxin Testing Solution
Available for On-demand Viewing
Data integrity plays a critical role in demonstrating adherence to GMP standards. Regulatory authorities expect accurate and dependable data across domains such as manufacturing, testing, and quality control.
Join our webinar to enhance your knowledge and skills in the realm of QC data integrity for endotoxin testing. Our expert speaker will guide you through practical strategies and tools to use to improve your lab’s data integrity.
- Data integrity essentials: Get an in-depth understanding of data integrity fundamentals and discover how it aligns with FDA corporate governance standards
- BET methods: Dive into the world of BET methods, with a special focus on automated test methods, and how they can improve your data integrity practices
- WinKQCL® Endotoxin Software: Explore the power of the WinKQCL® Endotoxin Detection & Analysis Software and learn how it simplifies compliance with FDA's data integrity guidance
- Assay process flow: Gain insights into the assay process flow, from meticulous sample preparation to the critical review and release of results
Who should attend:
- QC lab managers/supervisors/directors
- QC lab analysts
- QA managers
- Process development scientists
- Method development scientists
- Regulatory affairs managers
Speakers
Presenter
Josiah Hosie
Josiah Hosie
Product Strategist
Informatics
Lonza Bioscience
Informatics
Lonza Bioscience
Moderator
Shelton Sparks
Shelton Sparks
Product Manager
Testing
Lonza Bioscience
Testing
Lonza Bioscience
