Quality Control
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Maximizing Safety In The Daily Handling Of Hazardous Goods In The Lab
4/7/2022
Understand the role of safety in the lab as well as the challenges of handling hazardous goods and how you can overcome them.
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Making Sense Of Analytical Standards In Pharma QC
Reference materials are a critical component of the analytical testing workflow. Learn about metrological traceability, the hierarchy of reference materials, fit-for-purpose selection considerations, and more.
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Rapid Microbial Detection System For Earlier Results
4/7/2022
Learn about the Milliflex® Quantum system, a fluorescence-based microbial detection system that enables you to read results days earlier than traditional methods.
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Webinar On-Demand: Substitution Of Hazardous Substances
12/9/2022
Substitution is the essential starting point in every risk assessment. Learn how to conduct a legally compliant substitution check using real substances as examples.
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Determining CCI During Deep Cold Storage
7/23/2020
Deep cold storage, at dry ice (-80°C) or even cryogenic (-196 °C) temperatures, poses a significant challenge to packaging components and can result in CCI failures.
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Non-destructive Moisture Analysis Of Freeze Dried Product
1/2/2019
This webinar describes how non-destructive headspace moisture analysis can be used for characterizing batch moisture distributions, for lyo cycle development and optimization, and for freeze dryer moisture mapping and validation.
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The Future Of Robotics And Automation In QC In Microbial Testing Labs
4/7/2022
Automation based on the use of robotics and digital tools will transform the QC process in microbial testing labs to meet the productivity, data integrity, and reliability requirements of Pharma 4.0.
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Selecting Container Closure Components: Extractables And Leachables
Primary packaging components require a thorough assessment to ensure safety and efficacy. Plan ahead and start your assessment early to mitigate your risks, delays, and out-of-pocket costs.
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Using Positive Controls In Container Closure Integrity Studies
1/2/2019
This webinar describes the use of positive controls as an important element of CCI studies designed to validate packaging components for CCI or to qualify processes for producing good CCI.
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Container Closure Integrity Testing Method Development
Dr. Derek Duncan, Director of Product Lines, Lighthouse Instruments, covers approaches that can be used for method development for CCI testing in all phases of the product life cycle.