As with Europe, countries within Asia have specific translation requirements for computer software, Instructions for Use (IFU), packaging, and other Medical Device and Pharmaceutical labeling. In this ever-changing regulatory and international market clearance environment, it is vitally important for you to have this information at your fingertips. Without it you are unable to proactively properly plan your international market clearance strategy. In addition to the language requirements there are trends and country-specific requirements for the medical device directives and pharmaceutical regulations.
A comprehensive, easy-to-understand guide has been created in order to understand the necessary Asian language requirements for both Medical Devices and Pharmaceuticals.
A copy of this Asian language requirements document can be downloaded here free of charge.
Learn about what languages are required for marketing medical devices, IVDs and pharmaceuticals in Asia plus additional international language requirements including. Included in this helpful guide are:
- Medical Device and IVD Language Requirements
- Pharmaceutical Language Requirements
- Additional requirements and exceptions for medical devices
- Additional requirements and exceptions for pharmaceuticals
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