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MasterControl Deviations™

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Data Sheet 1 Data Sheet MasterControl Deviations™ In the FDA and ISO environments, the concept of quality is made tangible by written procedures and specifications, and any deviation from them must be documented and either justified or investigated. Such deviations may occur during sampling and testing, raw material and finished product acceptance, manufacturing, and product distribution. Effective investigation and resolution of deviations are an essential component of quality improvement and compliance. How Can MasterControl Software Solutions Help You? MasterControl Deviations automates and manages the process of documenting, investigating, and resolving operational deviations from written procedures and specifications. This solution provides the capability to resolve a deviation efficiently and to use data collected as a basis for continuous quality improvement. Continuous Validation™ MasterControl considers validation an integral part of software solutions for FDA-regulated customers. Our "continuous validation" approach dramatically cuts the time, pain, and cost involved in validation, making it easier to validate future upgrades. MasterControl's continuum of products and services address different levels of validation needs based on individual risk assessment. Here's how MasterControl addresses some of the major challenges that companies face when resolving deviations.

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