What does RDB (CDRH) mean in FDA
The Radiological Devices Branch (CDRH) is a division within the US Food and Drug Administration (FDA) that is responsible for approving medical devices related to radiation. The branch safeguards public health by ensuring the safety, effectiveness, and security of medical devices used in medical applications that involve radiation.
RDB (CDRH) meaning in FDA in Governmental
RDB (CDRH) mostly used in an acronym FDA in Category Governmental that means Radiological Devices Branch (CDRH)
Shorthand: RDB (CDRH),
Full Form: Radiological Devices Branch (CDRH)
For more information of "Radiological Devices Branch (CDRH)", see the section below.
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Essential Questions and Answers on Radiological Devices Branch (CDRH) in "GOVERNMENTAL»FDA"
What is the Radiological Devices Branch (CDRH)?
The Radiological Devices Branch (CDRH) is a division within the US Food and Drug Administration (FDA) that is responsible for approving medical devices related to radiation.
What does the CDRH do?
The CDRH safeguards public health by ensuring the safety, effectiveness, and security of medical devices used in medical applications that involve radiation.
Who oversees CDRH operations?
CDRH operations are overseen by FDA leadership.
How is CDRH funded?
CDRH is funded by user fees collected from manufacturers of certain radiologic products who register with the FDA.
Are there any restrictions on what products CDRH can evaluate?
Yes, only products related to imaging and therapeutic radiological activities are eligible for evaluation by CDRH.
Final Words:
By evaluating medical devices related to ionizing radiation, the FDA's Radiological Devices Branch (CDRH) ensures that these devices are safe and effective for use in medical procedures involving radiation. This helps protect public health and provides assurance to patients who rely on such products for their care.