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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. The concepts introduced here will be topics for future articles. initiatives. Industry 3.0

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Data Integrity in the Pharmaceutical & Life Sciences Industry

Viseven

All of it is done to assure data integrity—the glue that holds together all measures and actions performed to keep the data safe, error-free, and complete. In our new article, you will learn more about data integrity in the pharmaceutical and life sciences industry and why maintaining it matters so much.