The world of medical devices is going digital. Are you ready?
Some EU member states will accept labeling provided in English as long as the device is for professional use only. Learn more.
Find out about the pharmaceutical industry in CEE, the role of the European Medicines Agency (EMA), Russia and the new Russian pharmaceutical legislation.
Learn about the translation requirements driven by Croatia’s accession to the European Union.
Read about the current issues in pharmaceutical translations and finding the optimum translation process.
Learn about the Product Information Management system and the context in which writers and translators operate.
Watch this free webinar (54 min) to learn about best practices in document localization in the life sciences industry.
Learn about what it takes to achieve a successful clinical trial campaign in Latin America.
Learn about the most common globalization issues found in medical devices through visual examples.
Get information about Central and Eastern European countries and on managing translation requirements.
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