In this video, NSF expert Peter Wirthschaft, Ph.D., will guide IVD manufacturers through the new and most demanding aspects of the In Vitro Diagnostic Medical Device Regulation (IVDR) (EU) 2017/746.
Access NSF's IVDR resources at www.nsf.org/co....
For more information, contact us at www.nsf-prosystem.com.
Негізгі бет Changing Requirements for Manufacturers Under IVDR
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