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Cleaning validation calculations, conclusion and re-validation - Arabic.

Types of cleaning, cleaning mechanism, cleaning methods, optimization of cleaning procedures, worst case scenario, grouping strategy - Arabic.

The 30 minute webinar reviews a summary of quantitative and qualitative validation cleaning techniques for both FDA and non-FDA customers. It is followed by questions and answers submitted during the live telecast.

This video from GE Analytical Instruments highlights some key elements that can improve your cleaning validation program and will help you re-think the approach when using swabs for TOC analysis.

Cleaning validation video in a Slideshow mode.

Detailed description on pharmaceutical cleaning validation on a paper sheet - Hindi.

Validation of Cleaning Programs is now a mandatory requirement under most GFSI food safety standards. Luckily, Safefood 360° has compiled everything you need to know to keep your external auditors more than happy.

A Helpful introduction of computer system validation for beginners.

Validation is a broad concept in the pharmaceutical manufacturing industry. It includes process validation, analytical method validation, equipment validation, cleaning validation and system validation.

Process validation is establishing documented evidence which provides a high degree of assurance that a specific process will consistently produce a product meeting its predetermined specifications and quality characteristics.
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