Keep the GxP data integrity deck
Recall practical data-integrity moves for regulated biotech records.
Core recall ALCOA What does ALCOA force you to check? Objection The value is correct, so why keep the failed first run? Use when someone wants a clean record without the process trail. Your line The final value matters, but the record must show how we got there. Keep the failed run, document the reason for repeat, and link the final value to the source. Deleting the messy part makes the record less trustworthy, not more professional. It separates a valid correction from hidden reconstruction. Compare Good correction vs. risky overwrite A correction is defensible when the original record and…
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