New requirements in the ISO 14155 standard for Medical Device Clinical Investigations The ISO 14155:2020 (Clinical investigation of medical devices
Navigating the legal framework for placing Medical Devices (MD) and In Vitro Diagnostic medical devices (IVDs) on the EU market can seem complicated
The in vitro diagnostic (IVD) devices sold in the European Union require a CE mark to certify that the device complies with the current European
Do you want to place your medical device or in-vitro diagnostic device on the market, but you have limited resources to do so? We prepared this
ÅKRN is a European Medical Device and In-Vitro Diagnostics CRO that can help your company get clinical trial approval / EU market approval To
Checkout our LinkedIn profile.
Checkout our selection of resources about medical devices and clinical writing.
AKRN Social Network