Review of the Food and Drug Administration's Processes to Review Medical Device Submissions Under the Pre-Market Approval and Investigational Device Exemption Programs - Scholar's Choice Edition
from $14.75
The Medical Device R&D Handbook
$149.25
from $122.41
Violations Of 21 CFR Part 812 - Investigational Device Exemptions: Warning Letters Issued by U.S. Food and Drug Administration (FDA Warning Letters Analysis)
$160.00
from $156.00
Research Regulatory Compliance
$68.75
from $66.95
Significant and Nonsignificant Risk Medical Devices
from $108.29
Safety Evaluation in the Development of Medical Devices and Combination Products
from $26.00
Safety Evaluation of Medical Devices
from $65.37
More results from Amazon »