European Union Directives
A collection of European Union Directives from IHS that apply to medical devices.
This collection of European Union Directives applies to medical devices that are distributed and sold in the EU. The directives define essential requirements - such as the protection of health and safety - that goods must meet before being sold on the EU market.
Compliance with these directives is required to do business in the European Union, and the requirements contained in them are regulatory in nature.
Directives available in this collection include:
- Electromagnetic compatibility
- Low voltage equipment
- Medical devices
- Active implantable
- In vitro diagnostic