Changing Requirements for Manufacturers Under IVDR
NSF NSF
10.9K subscribers
765 views
0

 Published On Feb 15, 2022

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 https://www.nsf.org/consulting/health....

For more information, contact us at www.nsf-prosystem.com.

show more

Share/Embed