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What is a DHR review?

DHRs Review and Compliance Division reviews federal and state projects that may impact historic and cultural resources, and provides recommendations for protecting and preserving these resources.

What is a DHR form?

The FDA mandates that medical device companies produce a device history record (DHR) that contains all documentation related to manufacturing and tracking the device, and demonstrates that the device was manufactured ing to the information in the device master record.

What is the purpose of DHR?

The Device History Record (DHR) is an essential component of quality management, serving multiple functions that ensure compliance, traceability, and quality assurance in medical device manufacturing.

What is Alabama DHR?

The mission of the Alabama Department of Human Resources is to partner with communities to promote family stability and provide for the safety and self-sufficiency of vulnerable Alabamians.

What is a DHR record?

A Device History Record (DHR) contains all the documents that are related to the manufacturing and tracking of a medical device. US Food and Drug Administrations (US FDA) 21 CFR Part 820 mandates the manufacturers to maintain a DHR for each batch, unit, or lot.