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FDA’s Office of Pharmaceutical Quality Releases a White Paper on the Economics of Quality Management Incentives

The FDA's Office of Pharmaceutical Quality is pleased to announce the release of our new white paper: "Quality Management Initiatives in the Pharmaceutical Industry: An Economic Perspective" (July 2025).

This comprehensive analysis demonstrates that strategic investments in quality management initiatives deliver measurable returns for both companies and public health:

  • Economic Returns: Companies can realize significant cost savings through reduced defects, decreased waste, and improved operational efficiency. Even incremental investments in quality management can yield positive returns.
  • Public Health Benefits: Mature quality management practices help prevent drug shortages, strengthen supply chain reliability, and ensure consistent medication availability for patients. The paper quantifies the extensive costs of poor quality management - from direct manufacturing impacts to broader societal consequences.
  • Scalable Implementation: The economic model shows that quality management investments are not "all-or-nothing" — companies can implement stepwise approaches tailored to their specific context and resource levels.

The white paper includes real-world case studies, economic modeling, and analysis of costs across manufacturers, patients, healthcare systems, and society. It reinforces FDA's commitment to encouraging mature quality management practices that benefit both business outcomes and patient care.

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EU: dibattito sulle regole della sicurezza chimica

All’evento organizzato dal gruppo ECR al Parlamento europeo, l’Agenzia europea per le sostanze...

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AIFA: Online il Rapporto sulle Attività dell'anno 2024

Il Rapporto, pubblicato sul portale dell’Agenzia, presenta i dati e le attività principali...

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Critical Medicines Act europeo, nuova proposta di legge per garantire fornitura farmaci e principi attivi

Esponenti del Parlamento europeo insieme alle principali organizzazioni dell’industria farmaceutica...

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EMA opens door to reliance on FDA GMP inspections conducted outside the US

The European Medicines Agency (EMA) has begun accepting the Food and Drug Administration’s (FDA)...

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