FDA 21 CFR Part 11 & GAMP 5: Overview and Compliance1. FDA 21 CFR Part 11 – Electronic Records & SignaturesScope: Applies to electronic records and signatures in FDA-regulated industries (pharma, biotech, medical devices, etc.).Key Requirements:Electronic Signatures: Must be unique, verifiable, and legally binding.Audit Trails: Systems must maintain secure, time-stamped audit trails for record changes.Data Integrity: Ensures...
Tuesday, April 1, 2025
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Salesforce Admin Interview QuestionsSalesforce Admin, Apex and LWC Interview Questions with AnswersDifferent types of relationshipsWhat are Sharing Rules?Profiles and Permission SetsRole Vs ProfileWhat are triggersDifference between a role and a profileHow do you set up field-level security?What...
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