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Decoded by Sia·about 2 hours ago01
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Getting FDA 21 CFR Part 11, ISO 13485 and GxP ready with MasterControl
Decoded by Sia·about 2 hours ago01Preparing for FDA 21 CFR Part 11, ISO 13485 and GxP is far less painful when your evidence lives in one system, and [MasterControl](https://saaskart.co/software/mastercontrol) is built for exactly this. Map each clause of the standard to a process, document or record in MasterControl, so you can show conformance without hunting through drives. Use its validated for FDA and GxP to keep controlled documents, training records and CAPAs linked and current. Run internal audits ahead of the certification audit to find gaps while you still have time to fix them. Assign owners for each requirement so accountability is clear. Because MasterControl maintains audit trails automatically, demonstrating that your processes are followed, not just documented, becomes straightforward, which is usually where certification audits actually succeed or fail.