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Evolving Quality Risk Management: A Deep Dive into ICH Q9 (R1) with Kevin O’Donnell (HPRA) on the Pharma Conversations Podcast

In a recent episode of the Pharma Conversations podcast, Kevin O’Donnell of the Health Products Regulatory Authority (HPRA) offered a detailed and thought-provoking ...
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Solstice Advanced Materials on Powering the Global Shift to Low-GWP Inhaler Propellants

Solstice Advanced Materials outlines its perspective on the transition to lowGWP propellants in an interview with International Pharmaceutical Industry Journal, focu...
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Terumo Pharmaceutical Solutions on Integrated CDMO Services

International Pharmaceutical Industry Journal speaks with Michele Guasti, Global Product Manager at Terumo Pharmaceutical Solutions Division. The discussion explores...
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PFAS and Pharmaceuticals: Why the Industry Can No Longer Afford to Wait

Few regulatory issues have the potential to reshape pharmaceutical manufacturing as profoundly as PFAS. Often referred to as "forever chemicals", per- and polyfluoro...
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Differences Between US and EU Pre- and Post-Market Regulatory Obligations

Typically, global companies developing innovative therapies are familiar with the differences between regulatory systems in the United States and European Union. In ...
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Why Predictive Analytics are Crucial for Effective EU-HTAR Implementation

The EU’s Health Technology Assessment Regulation (EU-HTAR) aims to introduce more harmonised, efficient and evidencebased assessments of new health technologies. How...
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