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Business · 27/01/2010Updated: 10/17/2026 · 1 min read

FDA Releases Guidance on Mechanical Calibration of Dissolution Apparatus for Drug Manufacturers

The Food and Drug Administration (FDA) has published a guidance document to help pharmaceutical manufacturers comply with regulations requiring regular calibration of laboratory equipment, specifically dissolution apparatus 1 and 2, to ensure accurate results.

Original source language: Federal Register — Health and Human ServicesOpen original release →

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