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Correspondence Between ISO 13485:2016 and 21 CFR Part 820 RMS Requirements10411 Corporate Drive, Suite 102, Pleasant Prairie, WI 53158 262.842.1250 262.842.1240 info rcainc.com science.com2Correspondence
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The US FDA may move refers to the process of the Food and Drug Administration potentially relocating or changing locations.
Any entity or organization that is part of the FDA's regulatory oversight may be required to file for the potential move.
The process for filling out the US FDA may move paperwork typically involves submitting forms and documentation related to the proposed relocation or change in location.
The purpose of the US FDA may move is to ensure that the regulatory agency is able to continue its operations effectively and efficiently in a new location.
The information that must be reported on the US FDA may move includes details about the proposed new location, reasons for the potential move, and any potential impacts on stakeholders.
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