Image: Supplied I3CGLOBAL , a leading global regulatory compliance consulting organization, has issued an urgent industry advisory highlighting the low level of awareness among IVD manufacturers regarding the mandatory compliance requirements under the EU In Vitro Diagnostic Regulation (IVDR) 2017/746 especially among companies whose devices were previously self-declared under IVDD and now fall under Class B and C requiring Notified Body involvement for the first time. Unde
