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Pharma Trends: The Return of the FDA Warning Letters [Simone Ammons] Simone (George) Ammons
Yan Kugel is joined by Will Moss founder and CEO of Seal, to talk about the critical need for automation in GXP processes. Will shares his expertise on balancing automation with human oversight, addressing data privacy concerns, and the future of quality management in the pharmaceutical sector. The Need for […]
Yan Kugel is joined by Simone Ammons, a dynamic engineer, technical writer, and entrepreneur who has navigated through diverse industries with finesse. She’s the founder of the QuneUp, a data-driven software tool that reduces equipment downtime and boosts productivity in the pharmaceutical industry. In this episode, we will be discussing […]
Yan Kugel is joined by Pavan Pasupulati, the Vice President of Manufacturing Excellence at Caliber Technologies. Here, he shares valuable insights into the future of pharmaceutical manufacturing. With over 25 years of experience in both the process and IT industries, Pavan has become a key figure in driving digital transformation […]
In this podcast episode, Nagesh Nama shares his expertise in incorporating AI into validated processes within the pharmaceutical industry. He discusses the benefits, challenges, and best practices of using AI and machine learning technologies in pharmaceutical manufacturing quality.
Vasyl shares his expertise in integrating AI solutions into the pharmaceutical industry and the practical implications of driving innovation and growth. The conversation delves into the use of AI and machine learning models in pharma, including the application of large language models like ChatGPT and GPT-3 for employer education and […]
In this podcast episode you will learn about crucial parts of CSV that nobody teaches you during official training.
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.
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.
