ISPE Podcast: Shaping the Future of Pharma
ISPE Podcast: Shaping the Future of Pharma
Podcast Description
The International Society for Pharmaceutical Engineering’s ISPE Podcast: Shaping the Future of Pharma is ISPE’s newest platform for sharing the latest insights and thought leadership on pharmaceutical manufacturing, technology, and regulatory trends impacting the pharmaceutical industry. Join ISPE’s podcast host Robert Chew and our featured guests each episode to hear directly from the innovators, experts, and professionals driving progress for the industry and shaping the future of pharma.
Podcast Insights
Content Themes
The podcast covers critical themes such as pharmaceutical manufacturing advancements, AI integration in the industry, regulatory changes, and quality transformation. Examples of episodes include discussions on the role of AI in quality compliance with leaders like Magaly Aham from Takeda and insights on the latest challenges and opportunities presented by AI featuring Ben Stevens and Eric Staib.
The International Society for Pharmaceutical Engineering’s ISPE Podcast: Shaping the Future of Pharma is ISPE’s newest platform for sharing the latest insights and thought leadership on pharmaceutical manufacturing, technology, and regulatory trends impacting the pharmaceutical industry. Join ISPE’s podcast host Robert Chew and our featured guests each episode to hear directly from the innovators, experts, and professionals driving progress for the industry and shaping the future of pharma.
In this episode, Michelle Vuolo, Head of Quality at Tulip Interfaces and ISPE Good Practice Guide: Validation 4.0 co-lead, along with guide team member, Victor de Oliveira Silva Ferreira, Cruz, Project Manager for PEQMS – Implementation of Electronic Systems for the Quality Management System, Instituto De Tecnologia Em Imunobiológico/Fundação Oswaldo Cruz, join the podcast share their insights on how Validation 4.0 aims to leverage digital tools to transition from traditional validation methods to more dynamic, real-time processes. Explore how to utilize the principles of Quality by Design and Quality Risk Management to create dynamic, continuous validation practices, powered by digital innovations
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