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Considerations for safety data migration methods

European Pharmaceutical Review

During migration, the case processing team will manually enter the data using the outputs obtained from the source database, following the workflow configuration, to ensure accuracy within the target database.

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Methodology to Define a Pharma 4.0™ Roadmap

ISPE

Based on robust data flows, aspects and required controls can be assessed in detail—for example, manual data entry, interfaces between systems, media change, data conversion, data migration, and data archiving. Integration: A data set is digitized, centrally stored, and can be used by multiple processes.