According to the QSR, what is NOT a requirement for the record of a complaint investigation?

In the context of the Quality System Regulation (QSR), which governs the procedures and documentation required for medical device complaints, it is essential to consider what is specifically mandated for a thorough record of a complaint investigation.

The correct choice indicates that documentation regarding changes in procedures correcting quality problems is not explicitly required to be part of the record for a complaint investigation. Instead, the QSR emphasizes that the record should comprehensively document elements directly related to the investigation of the complaint itself. This means that the dates and results of the investigation, the nature and details of the complaint, and any replies to the complainant are crucial pieces of information that must be captured.

The rationale behind this is that the primary focus of the complaint record is to ensure the investigation is adequately documented to trace the cause and address the specific complaint raised. While changes in procedures may be a result of the investigation, they are not a requisite part of the immediate complaint record. This distinction underscores the regulatory emphasis on documenting the investigation itself over subsequent procedural changes that may arise from an analysis of the complaint.