Principles of In Vitro Diagnostic (IVD) Medical Devices Classification
The objective of the Working Group is to review and update the GHTF / SG1 / N045:2008 Principles of In Vitro Diagnostic (IVD) Medical Devices Classification document, taking into account the current level of development and experience in applying the risk-based approach to the classification of IVD medical devices.
The goal is to promote global harmonization in the premarket review processes.