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US FDA Announces PreCheck Implementation Roadmap

The U.S. Food and Drug Administration announced that it will begin accepting applications on February 1, 2026 for the PreCheck Pilot Program. This program will strengthen the domestic pharmaceutical supply chain by increasing regulatory predictability, facilitating the construction of manufacturing sites in the U.S., and streamlining aspects of pharmaceutical manufacturing facility assessments in advance of a specific product application.  

The PreCheck Pilot Program will select an initial cohort of new pharmaceutical manufacturing facilities and begin conducting PreCheck activities in 2026. These facilities will be selected based on overall alignment with national priorities such as products to be manufactured, phase of facility development, timeline to producing pharmaceutical products for the U.S. market, and innovation in facility development. Additional details will be released on the application website on February 1, 2026. ..[FDA]

28

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Industry wants more streamlining following recent EU reforms

While the European Union is undergoing major reforms to its regulation of medical devices, diagnostics,...

28

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FDA official offers tips on leveraging AI in drug manufacturing

Tina Kiang, director of the Division of Regulations and Guidance in the US Food and Drug Administration’s...

28

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Testo unico legislazione farmaceutica. La delega torna a Palazzo Chigi

1 | Farmaceutica, bozza ddl delega: tetti di spesa, payback e digitalizzazione   Il disegno di legge...

27

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Tariff Uncertainty Drives Short-Term Manufacturing Surge as Global Pharmaceuticals Enter Fragmented Growth Phase

lobal pharmaceutical output surged in 2025 due to preemptive production ahead of U.S. tariff actions,...

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