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Glossary Term
Device Accountability
Definition
Device Accountability refers to the processes and systems implemented to track and document the handling, usage, distribution, and disposal of medical devices throughout their lifecycle. In clinical trials and commercial use, device accountability ensures that every device is accounted for to maintain compliance, safety, and integrity.
Relevance to the MedTech Industry
Device accountability ensures transparency, traceability, and compliance with regulatory requirements. It safeguards patient safety by preventing misuse, improper handling, or unauthorized distribution of devices, particularly those used in clinical investigations or high-risk applications.
Additional Information & Related Terms
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