While translating labeling for medical devices designed for lay users in the EU is a given and effectively non-negotiable, a certain degree of latitude exists for medical devices 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, as well as about finding medical translators and reviewers in CEE.
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.