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GMP Cleanroom Routine Environmental Monitoring & Therapeutic Vaccine Final Product Testing | 4th March 2021

March 4 @ 3:00 pm - 4:00 pm


GMP Cleanroom Routine Environmental Monitoring: Learn from the British Standards expert to the ISO Committee for ISO 14644-1:2015 about the GMPs and WHO rules for Cleanroom Classification and Routine Monitoring and how the new MET ONE 3400+ from Beckman Coulter can help with Data Integrity issues of Routine Environmental Monitoring

Therapeutic Vaccine Final Product Testing: Learn about the challenges of testing therapeutic vaccines to USP<787> and how the HIAC 9703+ from Beckman Coulter can help overcome these challenges

Why Attend:
+ Learn about the GMPs and WHO rules for cleanrooms and the ISO 14644-1:2015 standard.
+ Understand the difference between cleanroom Classification and Routine Monitoring.
+ Learn how the new MET ONE 3400+ from Beckman Coulter can help with Data Integrity issues of Routine Environmental Monitoring programs
+ Understand which types of vaccines can use the USP<787> test for product release
+ Learn how the HIAC 9703+ from Beckman Coulter can help overcome the challenges of using USP<787>

Speaker:
Tony Harrison, Senior Manager, Beckman Coulter
(Former UK expert to ISO Committee for ISO 14644-1:2015)

Organizer

EP – Beckman Coulter Life Sciences

Venue

Live Webinar
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