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Argos Multilingual 5 min. read
How Have the EU MDR and IVDR Changed Clinical Investigations?

The European Union’s Medical Device Regulation (EU MDR) and In Vitro Diagnostic Regulation (IVDR) have brought about significant changes to clinical investigations of the devices that they regulate. In the context of the European Union Medical Device Regulation (EU MDR, Regulation (EU) 2017/745), “clinical investigations” refer to systematic studies conducted on human subjects to assess […]

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Argos Multilingual 5 min. read
Enhance Patient-Centered Care with Multilingual Communication 

Patient-centered care is a core principle in modern healthcare. In the most basic terms, patient-centered care emphasizes that healthcare should be tailored to each patient’s unique needs, preferences, values, and circumstances. This approach has been shown to significantly improve healthcare outcomes, creating environments where patients feel valued, understood, and are more engaged in their care. […]

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Argos Multilingual 5 min. read
Why is Localization Essential for Regulatory Compliance?

In today’s international business landscape, the ability to communicate clearly and comply with local regulations is not just beneficial—it’s essential to doing business in the first place. Globalization offers businesses unprecedented opportunities to expand their reach across borders, tapping into new markets and consumer bases. However, these types of opportunities require navigating complex local laws, […]

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Argos Multilingual 4 min. read
What Is the European Free Trade Association (EFTA) and How Does It Affect MDR + IVDR?

Consisting of Iceland, Liechtenstein, Norway, and Switzerland, the European Free Trade Association (EFTA) is a regional trade association that plays a key role in shaping trade dynamics, particularly within the European Union (EU). Despite not being EU members, EFTA countries align their regulations closely with the EU to ensure seamless trade and regulatory cooperation. This […]

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What Is the European Free Trade Association (EFTA)
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