News dal mondo
27
Mag
Generics drugmaker Sandoz calls for EU to probe alleged China dumping
Sandoz has asked the European Commission to investigate Chinese imports of amoxicillin trihydrate, alleging unfair state subsidies and non-market pricing, The Financial Times reported Friday. The drugmaker said Chinese imports undercut EU prices by about 47% and risked increasing European dependence on China for antibiotic ingredients. The complaint requested corrective measures and additional duties to prevent subsidised imports from flooding the market. IQVIA data cited in the complaint showed that about 80% of amoxicillin active pharmaceutical ingredients are imported from Asia. Sandoz said the Commission had not yet responded to the submission and requested priority review despite a full anti-dumping investigation potentially taking a year. China’s foreign ministry previously rejected claims of overcapacity and said protectionism would not improve competitiveness. [Financial Times]
22
Mag
Min. Salute - Strategia nazionale sulla salute e sicurezza sul lavoro, approvata in Conferenza Stato-Regioni
La Conferenza Stato-Regioni ha approvato il 21 maggio 2026, tramite accordo formale, la Strategia nazionale...
22
Mag
Testo unico farmaceutica, i lavori entrano nel vivo: a breve l’esame dei 302 emendamenti
...L’iter del provvedimento è ormai prossimo a entrare finalmente nel vivo, con l’esame...
18
Mag
AIFA Sistema informatico Workflow Officine Materie Prime - Ulteriore Aggiornamento tecnico 18 maggio 2026
Formati files ammessi: PDF editabile o p7m. Scansioni a 200 dpi, anche in bianco e nero, per ottimizzare...
15
Mag
US FDA’s New AI-Informed Inspection Pilot and What It Means for Industry
We have written on this blog about FDA’s modernization agenda from several angles lately—from...
le ultime news
11 Mar
EU Finalizes Pharma Reform Package, Clarifies New Rules On Modular Market Protection
11 Mar
PFAS restriction proposal: ECHA’s Socio-Economic Analysis Committee agrees its draft opinion
11 Mar
Farmaci - Gemmato: In cantiere anche un ritorno nazionale alla chimica farmaceutica di base
11 Mar
EMA outlines methods for evaluating supply chain vulnerabilities
09 Mar
US FDA drafts guidance on best practices for responding to inspection observations
09 Mar
Intelligenza Artificiale e salute: le agenzie regolatorie al centro della rivoluzione farmaceutica
06 Mar
Testo unico Legislazione Farmaceutica,: assegnato alla X Commissione Senato
04 Mar
ECHA’s Risk Assessment Committee adopts its opinion on PFAS restriction proposal