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Modernizing Pharmaceutical QC Laboratories: From Locked Data to AI‑Powered Decisions [Jon Welsh] Jon Welsh
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Reducing Risk and Costs: Continuous Water Quality Monitoring in Pharmaceutical Production [Konrad Sägesser] Konrad Sägesser
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Overcoming Tech Transfer Bottlenecks: From Paper Trails to Standardized Digital Hubs [Nikki Bishop] Nikki Bishop
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Transforming Pharmaceutical Development with Active Packaging [Badre Hammond] Badre Hammond
Risk Management is a critical topic that is, unfortunately, misunderstood by many pharmaceutical companies. Many take the reactive approach instead of the proactive one, and that can cause them a lot of money and risk customer lives.
Digital transformation is the future of the pharmaceutical industry. Having an electronic quality management system (eQMS) in place means better efficiency, convenience, and compliance. However, the transformation is not a simple thing as it is a critical change for the quality system.
Jennifer talks and gives practical advice on how to perform a successful supplier or internal audit from start to finish.
In this episode of the Qualitalks Podcast, you will learn how to prepare for audits as a GMP and a GxP auditor.
The manufacturing of sterile drugs is a critical and essential process. For the process to conform to the strict GMP requirement, it is crucial to design every aspect of the manufacturing with high quality in mind.
Due to the COVID-19 situation, governments across the world initiated lockdown and quarantines. The lockdowns have a severe impact on pharmaceutical manufacturing across the globe.
