Regulator Spotlight
In a March 2025 webinar jointly sponsored by EFPIA, EUCOPE, EuropaBio, IFPMA, and Vaccines Europe, Egyptian Drug Authority’s Asmaa Fouad shared EDA’s “story of trust and transparency” in establishing reliance practices and the benefits that have been realized for post-approval changes. EMA’s Emer Cooke and Martin Harvey gave opening and closing remarks, respectively, in which they stressed the global importance of reliance tools and the key role EMA plays in sharing assessment outputs.
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ABOUT THE WEEKLY SUPPLEMENT
Along with a feature story on a presentation or panel discussion at a conference in which leading regulators address the challenges and developments in a key area of concern, our Weekly Supplements include a summary listing of the “Updates in Brief,” drug GMP warning letters and recalls, and EMA non-compliance reports that have been posted on IPQ’s website during the week. Subscribers can then click through to the full posting.
Also provided, where applicable, are links to the parts of in-depth stories and Monthly Updates that have been released during the week.
Appended to the issue is a chronological listing of the headlines of the featured regulator stories since IPQ began its Weekly Supplement series in February 2024. Also appended are the headlines of the in-depth stories that IPQ has released since 2020. Those of especially high relevance to the regulator insights provided in this issue are indicated with a red star. Click on the headlines to access the stories.