News dal mondo
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]
15
Ott
AIFA: Online il Rapporto sulle Attività dell'anno 2024
Il Rapporto, pubblicato sul portale dell’Agenzia, presenta i dati e le attività principali...
14
Critical Medicines Act europeo, nuova proposta di legge per garantire fornitura farmaci e principi attivi
Esponenti del Parlamento europeo insieme alle principali organizzazioni dell’industria farmaceutica...
10
EMA opens door to reliance on FDA GMP inspections conducted outside the US
The European Medicines Agency (EMA) has begun accepting the Food and Drug Administration’s (FDA)...
EDQM seeks feedback on plans to add glycol adulteration section to monographs
The European Directorate for the Quality of Medicines and HealthCare (EDQM) is holding a consultation...
le ultime news
10 Set
GMP UPDATING - EU Consultation on EudraLex Volume 4 - Good Manufacturing Practice Guidelines: Chapter 1 Pharmaceutical Quality System
09 Set
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)
12 Ago
AIFA - Novità rilascio, rinnovo e variazione AIC
11 Ago
FDA - Report on the State of Pharmaceutical Quality
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