How to Prepare Well for Regulatory Audits
In this episode, Yan Kugel has interviewed Paul Palmer on how to prepare correctly for a regulatory GMP audit.
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Preventing Alarm Fatigue in Life Science Facilities with EMS and Smart AI [Stephen Tierney] Stephen Tierney
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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
Quality
Who Are Qualifyze and What Is Their Mission?
At Qualistery, we love talking to innovators within the pharmaceutical world. In this episode, Yan Kugel interviewed Florian Hildebrand and Carla Peraferrer. Florian is the CEO, and Carla is the Head of Quality at Qualifyze (formerly ChemSquare), a start-up that wants to change the way you conduct audits and qualify [...]
Why Data Integrity Is More Important Than Ever
Data integrity is a big deal nowadays, and many companies get warning letters due to nonconformities in this area. In this podcast, Daniel Milek, a Data Integrity expert, explains what data integrity is and how to maintain it correctly. (YouTube Video Below) Here are some of the discussed topics: 💡 [...]
How to Combat the Two Major Deficiencies in Pharma
Yogesh Krishan Davé has been working in the pharmaceutical industry for more than 40 years now. He is an EU Qualified Person and a consultant. During this long time, Yogesh has encountered many deficiencies from which most pharma companies suffer. In this podcast, Yogesh has addressed deficiencies in two [...]
When You Deal With Risk, Don’t Be a Firefighter!
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.
How to Choose and Implement the Right eQMS for Your Company
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.
How To Successfully Conduct and Document an Audit
Jennifer talks and gives practical advice on how to perform a successful supplier or internal audit from start to finish.
How to Prepare for an Audit as a GxP Inspector
In this episode of the Qualitalks Podcast, you will learn how to prepare for audits as a GMP and a GxP auditor.
How to Design Aseptic Manufacturing for Best Compliance
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.
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