Lessons Learned from FDA's Regulation of 'Single-Use' Device Reprocessing

Lessons Learned from FDA's Regulation of 'Single-Use' Device Reprocessing

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The Spring 2016 edition of AAMI Horizons is out now and features an article by AMDR’s Dan Vukelich entitled “Lessons Learned from FDA’s Regulation of ‘Single-Use’ Device Reprocessing.”  

The article explores a wide range of relevant topics including the scope of FDA guidance, SUD reprocessor compliance, the benefits of regulation, and the latest updates on the SUD reprocessing industry.

 

 

 

 

 

 

 

 

 

To learn more about AAMI, or to purchase the online issue, click here.

 

 

By |2017-09-06T17:46:07+00:00April 12th, 2016|Blog, In the Press|Comments Off on Lessons Learned from FDA's Regulation of 'Single-Use' Device Reprocessing