FDA QSIT - Quality System Inspection Technique
FDA QSIT (Quality System Inspection Technique) is the name of the document that provides guidance to the FDA field staff on the inspection process used to assess medical device manufacturer's compliance with quality system regulations.
An FDA QSIT inspection is a "top-down" inspection (vs. a "bottom-up" inspection) and rather than focusing on many minor deviations will focus on systemic issues that can primarily be detected within quality-related documentation and subsequent document sampling.
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Prepare Your Company for an FDA QSIT Inspection
An FDA quality system inspection technique audit focuses primarily on four major subsystems and their respective documentation samples and is an efficient way to determine systemic weaknesses. When an investigator conducts an FDA QSIT inspection, medical device companies can expect shorter audits and more serious repercussions---especially to upper management.
Documentation Must be Controlled Before a FDA QSIT Inspection
To prepare your company for a FDA QSIT inspection, documentation must be controlled and continually reviewed/compared against actual processes. Maintaining this level of document/process control requires advanced software solutions. MasterControl, a software company, specializes in document control, audit and process management solutions for highly regulated environments.
Learn More About FDA Quality System Inspection Technique
To learn more about FDA QSIT and the solutions that makes it easy to collaborate on, retrieve and store essential quality documentation, please feel free to contact a MasterControl representative.
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