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news

News from the world

09

Feb

Pharma expert discusses effort to standardize CMC quality information

The pharmaceutical industry and the US Food and Drug Administration (FDA) are collaborating on a structured data platform for submitting chemistry, manufacturing, and controls (CMC) information in new drug applications. This initiative is part of Project PRISM, which is the FDA’s regulatory cloud submissions platform...[RAPS]

09

Mar

US FDA drafts guidance on best practices for responding to inspection observations

The US Food and Drug Administration (FDA) has released a draft guidance detailing how manufacturers should...

09

Mar

Intelligenza Artificiale e salute: le agenzie regolatorie al centro della rivoluzione farmaceutica

L’introduzione dell’Intelligenza Artificiale (IA) nella medicina e nella farmaceutica sta...

06

Mar

Testo unico Legislazione Farmaceutica,: assegnato alla X Commissione Senato

La V Commissione Bilancio del Senato della Repubblica ha espresso parere favorevole al disegno di legge...

04

Mar

ECHA’s Risk Assessment Committee adopts its opinion on PFAS restriction proposal

The European Chemicals Agency’s (ECHA) Risk Assessment Committee (RAC) has concluded its evaluation...

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