A few short months from now, manufacturers of Class III medical devices must comply with FDA’s unique device identification (UDI) rule. Part 1 of this series focused on the need for companies to start ...
The Food and Drug Administration’s science-based mission includes receiving, generating and reviewing a wealth of data and products from the vast array of manufacturers and firms that the agency ...
Certain research funding programs restrict the number of applications an institution may submit. To ensure a fair and strategic selection process, SFU uses an internal limited submission process ...
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