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Pharma Trends: The Return of the FDA Warning Letters [Simone Ammons] Simone (George) Ammons
Borislav Milev is a CSV expert. In this podcast episode, he explains what cloud computing is and how to validate it in a GMP environment.
Risk management is a crucial part of the pharmaceutical quality management system. Unfraternally, many companies don’t get it right and don’t understand how to use ICH Q9 correctly. In this podcast episode, Alex hall explains the right way to approach risk and which tools to use
In this podcast episode, Daniel Milek, a CSV expert from Data Integral Ltd, provides precious guidance on how you should go about your system validations.
In this podcast episode, Paul Palmer explains what types of deviations are there and how to deal with them successfully.
Working in a permanent job has its benefits, but also being an independent contractor or consultant. This work can be fantastic for many people who work in the pharmaceutical industry, but want a change in pace or just had enough of organizational politics.
In this episode of The Qualitalks Podcast, Yan Kugel talked to Dr. Rhett Pascual, Ken Toley, and Dr. David Guy Brizan. They are the team responsible for CALIDAD.AI, a company changing how GMP inspectors will conduct their audits.
In this episode, Yan Kugel has interviewed Paul Palmer on how to prepare correctly for a regulatory GMP audit.
