Secure required certification by meeting performance and safety standards
Find the latest standards and European Union Directives for medical devices and products. The Medical Industry Collection provides a comprehensive collection of international regulatory material pertaining to device use and manufacturing. The EU Directives are a key component to attaining a CE Mark, necessary for products entering the EU. These medical industry technical specifications assure you can:
- Ensure market share
- Enhance product safety & effectiveness
- Access consolidated standards research sources