Mexico is the 4th largest user of Medical Device technology in the Americas. If it is a strategic target market for you, be careful; all medical devices must follow labeling requirement found in NOM-137-SSA1-2008! Labeling and instructions for use must be submitted in Spanish.
The Saudi Food & Drug Authority (SFDA) has issued new guidance on labeling requirements for medical devices approved for sale in the Kingdom of Saudi Arabia (KSA).
Westborough, MA, January 20, 2015 – GlobalVision International, Inc., a leading provider of Technical Translation Service specializing in medical translation, software localization, website globalization, marketing collateral translation, Multilingual Video & Audio, and transcreation, announces the results of its 15th annual customer satisfaction survey.
With international regulations for medical products becoming more rigorous, medical translation is becoming an essential component of successful product exportation and global system integration.
When it comes to medical documents translation, variations in procedures can make localization a daunting task for any medical-device manufacturer, medical software solutions provider, pharmaceutical company, clinical research organization or healthcare services provider.