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European Union Directives, covering medical devices, are standards that govern product efficacy and safety. Devices must meet or exceed these regulations for use throughout the EU. Adhering to these standards enables you to:
| Full Online Standards Solution | Individual Standards |
|---|---|
| Multiple standards | Minimal standards |
| Frequent purchases ($3000+/year) | Infrequent purchases |
| Standards access or budget management, organization-wide | Less than 5 employees use standards |
| Learn more about Engineering Workbench by IHS Markit | Buy now |
Millions of lives are saved by blood transfusions and this company plays a vital role in making transfusions safe. To provide hospitals with the best pre-transfusion diagnostic products, its researchers are identifying next-generation concepts and generating important innovations while also resolving problems and documenting their findings more efficiently.
One of the world’s premier semiconductor companies increased the number of cross references in its parts database from 100,000 to nearly 2 million. In doing so, the company boosted results of its parts with the lowest searches by 52 percent and helped its customers find alternatives for obsolete parts so they can avoid the need to redesign products.
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