Packaging changes could result from proposed device ID rule

01/1/2013 | Packaging World online

The FDA's proposal to set up a unique device identifier system for medical technologies will compel most firms to modify their packaging lines, which could be costly, according to this article. The FDA Safety and Innovation Act mandates that a final rule on the proposal be issued in the middle of May, not the middle of June, but the agency does not seem certain of satisfying either deadline, an industry official said.

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