Countless Warning Letters or FDA 483s include the following violations: “Failure to ensure, where the results of a process cannot be fully verified by subsequent inspection and test, that the process ...
The data generated using analytical test methods is essential for many of the critical decisions made in the pharmaceutical industry. To be confident in the integrity of this data it is crucial that ...
What will you learn on this course? This course looks at method validation from start (initial planning) to finish (on-going tracking of performance statistics). Starting with describing the end goal ...
Validation documentation should define process parameters, monitoring strategies, and operating ranges that can support ...
Excel’s data validation feature is more versatile than you might think. Learn how to use literal values, input values, list values, and even formulas to restrict input date values using data ...
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