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News from the world

29

Jan

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]

15

Apr

Difendere il valore della chimica-farmaceutica nazionale significa difendere il diritto alla salute del cittadino italiano

Nella seconda uscita della rubrica Ipse dixit, Marcello Gemmato (Ministero Salute) affronta i nodi della...

14

Apr

Farmaceutica, surplus Ue a 221 mld nel 2025: Italia prima per import

Nel 2025 l'Unione europea ha esportato prodotti medicinali e farmaceutici per un valore di 366,2...

10

Apr

“Difenderemo il farmaco made in Italy” - Sottosegretario alla Salute Gemmato: Dal payback alla dipendenza da India e Cina

“Mitigare il payback” che pagano le aziende farmaceutiche per rendere più attrattivo...

10

Apr

Contract manufacturing deals for drugs marketed in US shift to Europe

Biopharma companies are increasingly choosing to outsource manufacturing for the U.S. market to European...

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