All posts by Karen Fleshman

Karen Fleshman is co-founder and COO of Haskins Advisory Group (Haskins), a GS1 Standards and Global Unique Device Identification Database (GUDID) consulting and outsourcing company based in Chicago, IL., with over 10 years of experience in the Consumer Products, Foodservice, and Healthcare industries. Karen has extensive GS1 experience. Prior to the formation of Haskins, Karen worked for GS1 US where she led the Technology Support team and managed strategic accounts.

European Medical Device and In Vitro Diagnostic Medical Device Regulations Conference

Author Karen Fleshman

Once again I’ve asked Karen Fleshman, co-founder and COO of Haskins Advisory Group, to step in and cover the recent EU MDR and IVDR Conference that focused on Unique Device Identification (UDI).  I’ll return after the holidays with more coverage of pharma serialization.  Thanks Karen! –Dirk.

On December 4 – 6, 2017, the European Medical Device (MDR) and In Vitro Diagnostic Medical Device (IVDR) Regulations Conference was held in Orlando, FL. The conference was designed to educate, support, and assist US based medical device manufacturers in gaining critical insight on the requirements of the European Union (EU)’s Unique Device Identification (UDI) compliance program. Continue reading European Medical Device and In Vitro Diagnostic Medical Device Regulations Conference