סילבוס הקורס והתכנים צפויים להשתנות סמוך למועד פתיחת הקורס, בהתאם לעדכונים שיהיו ב-IVDR
The current Covid-19 pandemic showed the huge importance of good, safe and well performing In Vitro Diagnostic (IVD) tests: DNA – polymerase Chain Reaction (PCR) testing vs antigen tests.
Additionally, to the pandemic the in-vitro diagnostic (IVD)...המשך קריאה
סילבוס הקורס והתכנים צפויים להשתנות סמוך למועד פתיחת הקורס, בהתאם לעדכונים שיהיו ב-IVDR
The current Covid-19 pandemic showed the huge importance of good, safe and well performing In Vitro Diagnostic (IVD) tests: DNA – polymerase Chain Reaction (PCR) testing vs antigen tests.
Additionally, to the pandemic the in-vitro diagnostic (IVD) sector faces a significant challenge to plan for and comply with the new European IVD regulation (In Vitro Diagnostic Device Regulation (IVDR) EU 2017/746) before 26 May 2022.
The transition from the current IVD Directive to meeting the new requirements involves significant preparation and data generation to be ready for additional notified body review and scrutiny.
It is vital that IVD manufacturers get started and ready to fully understand the requirements of the IVDR and calibrate how to meet the new expectations.
This course provides insights in the overall IVDR requirements and how to comply to it through hands-on interactive examples and discussions with the audience addressing all questions of them as well.
סגור