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07

Ago

IPEC Risk Assessment Guide for Pharmaceutical Excipients

Availability of the IPEC Risk Assessment Guide for Pharmaceutical Excipients – Risk Assessment for Excipient Manufacturers (Version 1, 2025).

The IPEC Risk Assessment Guide provides detailed guidance on evaluating risks to excipient quality, supporting excipient manufacturers and distributors in making consistent, risk-based decisions, and serves as a resource for excipient users assessing their suppliers’ risk strategies.

Key Risk Assessment methodologies and tools for identifying and mitigating quality-related risks are outlined; this document is essential to understand and apply effectively the risk assessment principles referenced in the IPEC-PQG GMP (Good Manufacturing Practices) and IPEC GDP (Good Distribution Practices) Guides for Pharmaceutical Excipients.

24

Ott

ECHA & REACh - SMEs to apply for company size validation before making REACH submissions

The European Commission has adopted the revised REACH Fee Regulation. Micro, small, and medium-sized...

24

Ott

Changes to e-submission requirements for CEP applications for 1 November 2025

The European Directorate for the Quality of Medicines and HealthCare (EDQM) has published the requirements...

24

Ott

US FDA Publishes Filing Checklists to Prevent Submission Delays

The US Food and Drug Administration (FDA) published the internal checklists its staff reference when...

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