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Num Mark Subjects (1-10 of 10) Year Entries
38 Found
1 Device Approval.   12
2 Device Approval -- legislation & jurisprudence   8
3 Device Approval -- legislation & jurisprudence -- United States : Development of FDA-regulated medical products : a translational approach / Elaine Whitmore  2012 1
4 Device Approval -- legislation & jurisprudence -- United States -- Guideline : The FDA and worldwide quality system requirements guidebook for medical devices / compiled and written by Amiram Daniel & Ed Kimmelman  2008 1
5  

Device Approval, New -- See Device Approval


Process that is gone through in order for a device to receive approval by a government regulatory agency. This includes any required preclinical or clinical testing, review, submission, and evaluation of the applications and test results, and post-marketing surveillance. It is not restricted to FDA
  1
6  

Device Approval Process -- See Device Approval


Process that is gone through in order for a device to receive approval by a government regulatory agency. This includes any required preclinical or clinical testing, review, submission, and evaluation of the applications and test results, and post-marketing surveillance. It is not restricted to FDA
  1
7  

Device Approval Processes -- See Device Approval


Process that is gone through in order for a device to receive approval by a government regulatory agency. This includes any required preclinical or clinical testing, review, submission, and evaluation of the applications and test results, and post-marketing surveillance. It is not restricted to FDA
  1
8 Device Approval -- standards   11
9  

Device Approvals -- See Device Approval


Process that is gone through in order for a device to receive approval by a government regulatory agency. This includes any required preclinical or clinical testing, review, submission, and evaluation of the applications and test results, and post-marketing surveillance. It is not restricted to FDA
  1
10  

Device Approvals, New -- See Device Approval


Process that is gone through in order for a device to receive approval by a government regulatory agency. This includes any required preclinical or clinical testing, review, submission, and evaluation of the applications and test results, and post-marketing surveillance. It is not restricted to FDA
  1
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