News dal mondo
21
Apr
TGA clarifies therapeutic goods are unaffected by chemical production and import ban
TGA has clarified the impact of Australia’s industrial chemicals standards on medicines, medical devices, and biologicals. Responding to stakeholder queries, TGA said therapeutic goods are not affected by prohibitions imposed under the Industrial Chemicals Environmental Management Standard (IChEMS). The framework prohibits the import, manufacture, and use of specified chemicals in Australia. Certain PFAS chemicals, UV-328, and Dechlorane Plus are among the chemicals covered by IChEMS. TGA said IChEMS does not apply to chemicals used for therapeutic purposes. That limitation of the standard’s scope extends to the primary and secondary packaging of medicines and biologicals, as well as to the primary packaging, instructions for use, and spare parts of medical devices. The agency posted two statements about the exemption of medical devices from the PFAS ban last year. While TGA’s second statement clarified that medicines and biologicals are exempt from the ban, neither notice addressed chemicals other than PFAS. [RAPS]
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
22 Mag
Min. Salute - Strategia nazionale sulla salute e sicurezza sul lavoro, approvata in Conferenza Stato-Regioni
22 Mag
Testo unico farmaceutica, i lavori entrano nel vivo: a breve l’esame dei 302 emendamenti
18 Mag
AIFA Sistema informatico Workflow Officine Materie Prime - Ulteriore Aggiornamento tecnico 18 maggio 2026
15 Mag
US FDA’s New AI-Informed Inspection Pilot and What It Means for Industry
15 Mag
EU Regulators discuss new pharma legislation, AI, and more
15 Mag
US FDA official details top observations from QMSR inspections
15 Mag
European Commission outlines plans to mobilize EMA to diversify supply chains
13 Mag
Deal on tackling EU shortages of essential medicines