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News dal mondo

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]

06

Feb

US FDA proposes waiving GDUFA facility fees for domestic manufacturers

The US Food and Drug Administration (FDA) has proposed waiving annual facility fees for the first three...

06

Feb

Computer Software Assurance for Production and Quality Management System Software

FDA is issuing this guidance to provide recommendations on computer software assurance for computers...

04

Feb

FDA, EMA officials encourage companies to pilot eCTD 4.0

Companies should increase their efforts to address issues and test their electronic Common  Technical...

03

Feb

China revises drug administration regulations to spur innovation, tighten oversight

Entrano in vigore il 15 maggio 2026 le nuove norme che aggiornano in profondità la legge sui...

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