European Pharmaceutical Review
SEPTEMBER 26, 2023
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.
ISPE
JUNE 21, 2023
Software applications were just beginning to be deployed to capture data that supported predicate rules and regulatory submissions. The industry needed definitions and guardrails to ensure consistency and assurance that the data being captured had data integrity and the right levels of control points (i.e.,
ISPE
MAY 11, 2023
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. Good Practices for Data Management and Integrity in Regulated GMP/GDP Environments.”
Expert insights. Personalized for you.
92 
Let's personalize your content