The traceability of data provided by the Quality control lab, within the pharmaceutical industry, is critical chain for the safe release of products. As a result, looking at ways to improve data integrity continues to be a topic of discussion.
In this webinar, we address what are the specific challenges associated with microbiology and related documentation, and how the current technologies and digitalized solutions help smooth over those hurdles.
It includes the following agenda topics:
- Challenges linked to Data Integrity in Pharma QC labs
- Support of technologies and digitalization to:
- Decrease the workload of paperwork
- Provide mobility for testing at several locations
- Ensure traceability for a long period of time
- Workflow facilitation through digitalization
- Live Q&A
Speakers
Nicolas Lelievre
Merck
Regional Application & Commercial Tactics Manager, Western Europe
Nicolas holds a PhD degree in cell and tissue engineering and has 15 years of experience in industrial microbiology and validation. He has spent 12 years as a Validation Engineer, supporting our customers in the validation of both classical and rapid systems and methods for microbiological monitoring while also training operators as a certified trainer. Currently, he is responsible for driving regional commercial strategies for sterility testing applications and delivering comprehensive training on sterility testing to QA/QC teams across Europe.
Microbiological testing
- Sterility testing
Duration:1h
Language:English
Session 1:presented December 5, 2024
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