ISPE Podcast: Shaping the Future of Pharma

n this episode, listen to highlights from our most recent Artificial Intelligence-focused episodes, featuring discussions with speakers from the FDA, Sanofi, and the Open BioPharma Research and Training Institute on the potential for AI to reshape the drug lifecycle, how companies are leveraging artificial intelligence to drive quality transformation and accelerate workforce readiness, and more.

n this episode, listen to highlights from our most recent Artificial Intelligence-focused episodes, featuring discussions with speakers from the FDA, Sanofi, and the Open BioPharma Research and Training Institute on the potential for AI to reshape the drug lifecycle, how companies are leveraging artificial intelligence to drive quality transformation and accelerate workforce readiness, and more.

In this recap 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 insigh...

In this recap 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 insigh...

In this episode, Miguelina Matthews, Head of Quality Intelligence, Advocacy and Pharmacopoeia Affairs at Sanofi, joins the podcast to share how the company is leveraging artificial intelligence to shift pharmaceutical quality management from reactive investigations to predictive, data-driven insights. Learn more about the deployment of Sanofi's "Plai" tool, emphasizing the importance of robust gov...

In this episode, Miguelina Matthews, Head of Quality Intelligence, Advocacy and Pharmacopoeia Affairs at Sanofi, joins the podcast to share how the company is leveraging artificial intelligence to shift pharmaceutical quality management from reactive investigations to predictive, data-driven insights. Learn more about the deployment of Sanofi's "Plai" tool, emphasizing the importance of robust gov...

On this episode, David Estapé, Technology Manager Biotechnology at CRB Group GmbH, and International Program Committee Chair of the 2026 ISPE Europe Annual Conference, joins the podcast to discuss the upcoming conference and the topics, speakers, and key highlights of what you can expect from the educational content and agenda.

On this episode, David Estapé, Technology Manager Biotechnology at CRB Group GmbH, and International Program Committee Chair of the 2026 ISPE Europe Annual Conference, joins the podcast to discuss the upcoming conference and the topics, speakers, and key highlights of what you can expect from the educational content and agenda.

This episode features insights from Tina Kiang, PhD, Director of the Division of Regulations and Guidance in the Office of Pharmaceutical Quality (OPQ)/Office of Policy for Pharmaceutical Quality (OPPQ) at the US Food and Drug Administration (US FDA). In a discussion facilitated by David Churchward, Head of Operations Quality Compliance and External Affairs at AstraZeneca, Kiang examines AI at the...

This episode features insights from Tina Kiang, PhD, Director of the Division of Regulations and Guidance in the Office of Pharmaceutical Quality (OPQ)/Office of Policy for Pharmaceutical Quality (OPPQ) at the US Food and Drug Administration (US FDA). In a discussion facilitated by David Churchward, Head of Operations Quality Compliance and External Affairs at AstraZeneca, Kiang examines AI at the...

In this episode, Susan Szathmary and Richard Jaenisch, both of Open BioPharma Research and Training Institute, join the podcast to share how to accelerate the adoption of new technologies through applied AI in pharma manufacturing and for workforce readiness.

In this episode, Susan Szathmary and Richard Jaenisch, both of Open BioPharma Research and Training Institute, join the podcast to share how to accelerate the adoption of new technologies through applied AI in pharma manufacturing and for workforce readiness.

In this recap episode recorded after the 2025 ISPE Annual Meeting, host Bob Chew shares insights on accelerating technology adoption in the pharmaceutical industry. Dive into this discussion to explore the future of pharma innovation, including transitioning from document-centric to data-driven quality systems, leveraging AI and digital twins for enhanced manufacturing processes, and reimagining r...

In this recap episode recorded after the 2025 ISPE Annual Meeting, host Bob Chew shares insights on accelerating technology adoption in the pharmaceutical industry. Dive into this discussion to explore the future of pharma innovation, including transitioning from document-centric to data-driven quality systems, leveraging AI and digital twins for enhanced manufacturing processes, and reimagining r...

This episode includes highlights from our Future of ATMPs series, featuring speakers from last year's ISPE Europe Annual Conference discussing industrialization of Advanced Therapy Medicinal Products production by replacing manual, high-cost processes with standardized and modular automation.

This episode includes highlights from our Future of ATMPs series, featuring speakers from last year's ISPE Europe Annual Conference discussing industrialization of Advanced Therapy Medicinal Products production by replacing manual, high-cost processes with standardized and modular automation.

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...

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...

In this episode, listen to highlights from our Artificial Intelligence-focused episodes, featuring discussions on the current state of AI in the pharmaceutical industry, key AI-related challenges and opportunities, and how AI can enable sustainable quality transformation.

In this episode, listen to highlights from our Artificial Intelligence-focused episodes, featuring discussions on the current state of AI in the pharmaceutical industry, key AI-related challenges and opportunities, and how AI can enable sustainable quality transformation.

In this episode, host Bob Chew is joined by Martin Orcoyen, President of ISPE Argentina Affiliate, Ricardo Miranda, President of the ISPE Brazil Affiliate, and Alejandro Bustamante, President of the ISPE Mexico Affiliate, to discuss the jointly hosted 2025 ISPE LATAM Symposium.

In this episode, host Bob Chew is joined by Martin Orcoyen, President of ISPE Argentina Affiliate, Ricardo Miranda, President of the ISPE Brazil Affiliate, and Alejandro Bustamante, President of the ISPE Mexico Affiliate, to discuss the jointly hosted 2025 ISPE LATAM Symposium.

In this episode, host Bob Chew shares insights on accelerating technology adoption in the pharmaceutical industry. Dive into this discussion to explore the future of pharma innovation, including transitioning from document-centric to data-driven quality systems, leveraging AI and digital twins for enhanced manufacturing processes, and reimagining risk management with statistical tools.

In this episode, host Bob Chew shares insights on accelerating technology adoption in the pharmaceutical industry. Dive into this discussion to explore the future of pharma innovation, including transitioning from document-centric to data-driven quality systems, leveraging AI and digital twins for enhanced manufacturing processes, and reimagining risk management with statistical tools.

Scott Billman, Senior Vice President, Global Engineering, Technology, and Facilities at Solventum and Immediate Past Chair of the ISPE International Board of Directors, joins the podcast to share more about the upcoming ISPE Annual Meeting and Expo. Explore the featured topics, trends, and pharmaceutical innovations, as well as opportunities for networking and career advancement that you can expec...