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A SPECIAL
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DATE: May 31, 2018
TIME: 11:00 AM EDT
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DURATION: 1 Hour
HOST: Charles River
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One
of the first elements of any regulatory audit is to analyze and
scrutinize a firm’s investigation reports and review how they control
their manufacturing and laboratory processes. Considering this, it is
critically important for patient safety as well as quality compliance
that both investigations and how the firm demonstrates process control
is done right the first time.
In
this webinar, presented by subject matter experts at Biogen, we’ll
review real-world examples that showcase how they developed a plan for
utilizing the automation functionalities and data generation
capabilities with Cortex™.
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Have a scheduling conflict?
Sign up even if you can't make it; we'll share the recording after.
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Matthew Paquette, MBA
Product Specialist
Charles River
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Stephen Spence, Candidatus Scientiarum
Qualification SME
Biogen (Denmark) Manufacturing ApS
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Svend da Silva
Sr. Associate II, Global QC Operations
Biogen (Denmark) Manufacturing ApS
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RESERVE YOUR SEAT → |
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EUREKA BLOG
An online community to explore, connect, and share big ideas.
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THE SOURCESM
Unlock exclusive control data, scientific posters, presentations, and videos.
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WEBINAR ARCHIVE
Access the latest innovations and technical guidance.
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PORTALS
Secure platforms for convenient connection to your data.
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©2018 Charles River Laboratories International, Inc.
Charles River Laboratories | 1.877.274.8371 | 251 Ballardvale St. | Wilmington, MA | 01887
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