Drug Stability Tests

Drug Stability Tests

In drug development, products or substances must preserve their chemical, physical and microbiological properties. With pharmaceutical stability testing, slowing factors such as API degradation can be minimized.

Drug Stability Tests

EUROLABoffers international protocol standards and personalized solutions based on pharmacological stability services. We test APIs, raw materials and finished products under recommended environmental storage conditions such as Temperature, Humidity, Light and Time-Long Term / Accelerated. 

Our GMP certified laboratory system allows us to evaluate product quality at specific time intervals under controlled and monitored conditions. The stability test is supported by embedding chambers, thermal stability chambers, humidity control climate chambers and storage space.

Stability, Storage and Compatibility Tests

  • Stability
  • Packaging Compatibility
  • Storage services
  • Organoleptic properties - Appearance, color, odor, texture
  • Analytical services - Viscosity, color, odor / odor, pH, weight, active ingredients, Traces of Impurities, UV filters, Heavy metals, preservative analysis
  • Microbiological properties - Microbial count and microbial count
  • Functionality and Aesthetics

Stability Conditions

  • Real time
  • Accelerated under ICH or special climatic zones
  • Freeze-thaw cycle studies
  • Thermal stability
  • Light, Luminescence ICH Q1B

Stability Test Required Conditions

  • Pharmaceutical product development
  • Reorganization of remarketing products
  • Changing production methods
  • Production site is fast
  • Product packaging change

EUROLAB, with its highly expert team and internationally accredited laboratories, Drug Stability Tests It performs all test, analysis, measurement, evaluation and report generation services completely and reliably.

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