Compounding Data Entry Documentation FDA 
European Pharmaceutical Review
MARCH 12, 2024
Ensuring data integrity in the life science industry is crucial for regulatory compliance. Regulatory bodies such as the US Food and Drug Administration (FDA) and European Medicines Agency (EMA) place great importance on data integrity in the pharmaceutical/life science industry. Good documentation practices.
ISPE
JUNE 21, 2023
The ISPE Sub-Committee for Paperless Validation has defined ‘Paperless Validation Systems’ as Paperless solutions enable validation lifecycle deliverables to be generated, approved, and more importantly, testing to be completed without the need for the printing of paper test documents. If It Is Not Documented, It Did Not Happen.
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