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Here we will examine how EFTA is affected by the EU’s Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR).

In this blog post, we've shared the key points to consider before engaging in the social media sector in Japan.

Discover the key strategies for navigating the complexities of the Japanese market and achieving successful localization.

In this blog post we explain why LQA is so crucial in Japan and what are the biggest challenges of LQA for this country. 

Notified Bodies, appointed by EU member states, assess the conformity of medical devices and in vitro diagnostic products.

Learn how multilingual marketing is reshaping the life sciences industry. From patient-centered care to global accessibility, it's a game-changer.

Manufacturers of in vitro medical devices have an extended time of 31 months to adjust to the regulation