There are four opportunities to apply a Risk-Based Approach for Computer Systems Validation. These opportunities include utilizing risk to scale, supplier audit efforts, validation deliverables, testing and documentation levels. All...
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A standardized process is a well-defined and structured set of activities built for conception through retirement. Process Standardization creates transparency across the lifecycle framework and enables management control. It establishes...
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A well-defined Lifecycle Framework strategy is designed to create a uniform approach throughout the entire organization. The benefit of having a uniform approach reduces the amount of rework that will...
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The pharmaceutical and medical device industry is a rapidly changing environment. Successful businesses are those who are able to stay on top of the newest trends and regulations while aligning...
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The regulatory landscape is dynamic in nature, constantly evolving and changing at an accelerated pace. Keeping up with the changing regulations can be an uphill task for organizations in highly...
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Computer system validation (CSV) has become essential in the drug and medical device industry. The FDA defines process validation as "establishing documented evidence which provides a high degree of assurance...
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