Medical Device Industry and COVID-19: Regulatory Modifications to Consider

The COVID-19 pandemic has overwhelmed our healthcare delivery systems and has effected the delivery of medical care across the spectrum. Medical device companies have also been hit by the crisis
as they struggle to make decisions regarding supply chains, and regulatory obligations in the midst of uncertainty.
Please find our blog discussing the impact of the pandemic on medical device regulations.

EU MDR 2017/745

The European Economic Area (EEA), inclusive of the European Union (EU) and European Free Trade Association (EFTA), has been contemplated as one of the largest global medical device markets. The obvious aspiration for device manufacturers is gaining an approval and maintaining access to this important market. It requires abiding by the regulatory changes to assure…