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Webinars:
BioPharma
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DuPont™: Quality Risk Management for Cleanroom Garment Qualification in the Light of GMP Annex 1
The new GMP Annex 1, published on 22 August 2022, requires a wholistic QRM-based approach for pharmaceutical cleanrooms. It also requires a data driven and more thorough qualification of cleanroom garments. This webinar will show you how the new Annex 1 may be applied to cleanroom garments.
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Thermo Scientific: Cell Culture: Overcoming Challenges in GMP Environments
Optimise your culture yields the Thermo Scientific brand.
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Pall Pharma R&D Filtration Solutions
Innovative solutions for life science research workflows.
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Memmert: Stability Testing of New Drug Substances and Products Q1A (R2)
ICH guideline Q1A (R2) for registration purposes and emphasising topics such as stability testing, forced degradation studies and storage testing in combination with products to be used.
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Binder: Climate Chambers for Long-term Studies and Stress Testing
The Solid.Line series is especially designed for long-term ICH stability testing.
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Eppendorf: How to Gain Process Efficiencies with Your -80°C Storage with Advanced Ultra-low Temperature Freezers
Documentation and traceability are key elements of any workflow in your pharmaceutical laboratory.
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