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Actualizaciones regulatorias24 ago 2026•1 min de lectura

FDA Recalls Product Due to CGMP Deviations

Por el equipo de PharmaCountry

The FDA has initiated a recall of a product because of deviations from current Good Manufacturing Practices (CGMP).

The U.S. Food and Drug Administration (FDA) has issued a recall for a pharmaceutical product after identifying deviations from current Good Manufacturing Practices (CGMP). The recall underscores the agency's focus on ensuring manufacturing compliance and product safety.

Recopilado por el equipo de PharmaCountry · Fuente: FDA.gov