Laboratory Application
Validation
Validation activities establish documented evidence that equipment, methods, and processes consistently perform within defined specifications.
Application Overview
Validation in pharmaceutical laboratories encompasses equipment qualification (IQ/OQ/PQ), analytical method validation, and cleaning validation. All equipment used in GMP environments must be qualified before use, and analytical methods must be validated to demonstrate they are fit for their intended purpose.
Common Laboratory Activities
- Equipment Installation Qualification (IQ)
- Equipment Operational Qualification (OQ)
- Equipment Performance Qualification (PQ)
- Analytical method validation
- Dissolution method validation
- Calibration and verification programs
Relevant Equipment Categories
The following equipment categories are commonly used in Validation laboratory activities.
Disintegration Testers
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Tablet Hardness Testers
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Friability Testers
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Tap Density Testers
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Powder Testing Equipment
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HPLC Systems
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UV-Vis Spectrophotometers
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Laboratory Balances
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pH Meters
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Temperature Equipment
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Stability Chambers
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Ovens
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Incubators
Coming soon
Autoclaves
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Other Laboratory Equipment
Coming soon
Related Equipment
Equipment models available in categories relevant to Validation applications.
Other Applications
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