Best Practices for Localizing Medical Devices

Best Practices for Localizing Medical Devices

This is your guide to localizing your multilingual medical device content ready for exporting into global markets.

In this guide, you will learn all the basics that will help you understand the best practices for localizing medical device content supported with industry insights, market potential, regulatory considerations, and essential planning.

Why Read It? Exporting your medical devices to international markets requires ensuring they are safe and effective. In addition, because your medical device labels need to be translated and localized, you must make sure labeling is clear and understandable. Passing the painstaking standards for multilingual medical device labeling is tough. Achieving this requires accurate translation, localization, testing, and validation. This provides in-depth discussion to ensure your medical device content is ready for exporting on a global scale.
Key Insights and Takeaways
Growth drivers and significant trends behind the global medical device market. Market potential and regulatory requirements before bringing a medical device to market. The importance of regulatory considerations and implementing an effective regulatory strategy. Planning and preparation processes for translating, localizing, reviewing, and testing medical device content.
Work with Welocalize Life Sciences and NLG
Welocalize Life Sciences has expanded our global team of experts specializing in language services for medical device, diagnostic, and pharmaceutical companies by welcoming Next Level Globalization (NLG) – a provider of expert language services for global life sciences companies – into the Welocalize family.