News from the world
14
Jul
China NMPA conducts management review of QMS for regulation of vaccine and drug GMP compliance
The National Medical Products Administration (NMPA) conducted its 2025 annual management review of the Quality Management System (QMS) for regulation of vaccine and drug Good Manufacturing Practice (GMP) compliance on June 30. NMPA Commissioner Huang Guo presided over the meeting and fully affirmed the suitability, adequacy and effectiveness of the NMPA's QMS in both areas...[NMPA]
17
Jul
Inside Pharma’s Push for More Resilient Supply Chains
Industry leaders from Samsung Biologics and Fujifilm Biotechnologies discuss how regional manufacturing,...
17
Jul
US FDA CDER plans new guidance on AI, electronic safety report submissions, and more
The US Food and Drug Administration’s (FDA) Center for Drug Evaluation and Research (CDER) has...
16
Jul
EU DG SANTE and EMA sign Working Arrangement with New Zealand Ministry of Health
DG SANTE and the European Medicines Agency (EMA) have signed a Working Arrangement with New Zealand Ministry...
15
Jul
Riforma farmaceutica. Via libera della Commissione Sanità del Senato
Le poche modifiche approvate non cambiano l'impianto della riforma. L’articolo 3 a...
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13 Jul
Stupefacenti, nuova circolare del Ministero: regole su custodia, giacenze, responsabilità e registri
26 Jun
FIS di Montecchio Maggiore accelera il percorso di decarbonizzazione industriale
26 Jun
FIS accelera sulla sostenibilità: biometano e taglio del 63% delle emissioni entro il 2035
26 Jun
US FDA investigator, experts seek to dispel misperceptions around 483s
26 Jun
AIFA - Aggiornate le Q&A sui processi autorizzativi AIC
26 Jun
US FDA Issues FY2025 Report on the State of Pharmaceutical Quality
19 Jun
Acque reflue. Il Parlamento UE chiede la sospensione e la revisione della direttiva
19 Jun
Australian Regulator Floats Plan To Make GMP Inspection Results Public