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12
Ago
FDA’s program to speed up US manufacturing buildouts
While the agency’s PreCheck regulatory framework is a good first step, it remains to be seen whether the program boosts U.S. drug manufacturing, says former FDA official...[PharmaManufacturing]
19
Set
Farmaci, EU: priorità rimediare a carenze
Per la Commissione europea guidata da Ursula von der Leyen rimediare alle carenze di farmaci critici...
18
Corte Conti UE - Carenza di farmaci: le misure dell’UE hanno fornito un valore aggiunto, ma i problemi strutturali persistono
Nel 2023 e nel 2024 sono stati segnalati livelli record di carenze di medicinali nei paesi dell’UE L’Agenzia...
US FDA Commissioner Makary Renews Tough Talk About Instituting Unannounced Foreign Inspections
Foreign drug manufacturers are having a time of it these days. On top of the confusion and controversy...
10
GMP UPDATING - EU Consultation on EudraLex Volume 4 - Good Manufacturing Practice Guidelines: Chapter 1 Pharmaceutical Quality System
Eu European Commission Consultation - Stakeholders’ Consultation on EudraLex...
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US internal Mock DEA-Style and Mirror Inspections and Audits: Trust But Verify
08 Set
Min. Salute UCS 29 agosto 2025 - Precursori di droghe - Regolamento UE 2025/1475 che estende il controllo a 2 nuove sostanze - In vigore dal 14 agosto 2025
18 Ago
US GDUFA IV: Industry wants more transparency
US President signs executive order to fill the strategic stockpile of active pharmaceutical ingredients (APIs)
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