Request a Quote for IHS Medical Devices Standards Collections

The IHS Medical Devices Standards Collections were designed to ensure compliance to the European Union (EU) Directives that define the "essential requirements" (e.g., protection of health and safety) that goods must meet when they are placed on the EU market. It provides 24x7 access to vital industry standards from BSI, CEN, CENELEC, ETSI and other Standards Developing Organizations that are continually updated, and leverages sophisticated management tools to keep customers informed of standards critical to the design process. The collections contain the Directives and Harmonized Standards from the Official Journal of the European Union (EU) that supplement and interpret the requirements of the Directive.

Choose from the list of collections below, then enter the required information for a quote.

To speak with an IHS Subject Matter Expert call 1-888-752-0334, outside the US/Canada call 303-397-2892.

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Choose from the Collection list: Medical Devices General - (EU Directive 93/42/EEC) Medical Devices Active Implantable - (EU Directive 90/385/EEC) Medical Devices In Vitro Diagnostic - (EU Directive 98/79/EC) Medical Devices Active Implantable & In Vitro Diagnostic Medical Devices General, Active Implantable & In Vitro Diagnostic Medical Devices Electromagnetic Compatibility - (EU Directive 89/336/EEC) Medical Devices Low Voltage Equipment/Medical Subset - (EU Directive 73/23/EEC) Medical Devices Low Voltage Equipment/Complete - (EU Directive 73/23/EEC)