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Labeling Impact on Worldwide Market Clearance

labeling impact on  global marketThere are a few methods manufacturers can use to properly label their products and successfully gain market clearances worldwide. These different methods require consideration of the time, cost, and risk involved for your company. Common to all of them is the requirement for translation of the labeling. For all major markets, and many emerging markets, the product labeling is required to be in the country’s official language. Depending on your approach, your market clearance registration dictates where the responsibility for translation lies. Review and control of the finished label, and the risks involved if the translation is incorrect, are considerations that every manufacturer must factor into their market clearance planning.

For the methods described in this report there are certain import/export requirements that must be considered. Manufacturers based in the United States must either register the product internationally using the same product code used for their domestic registration, or they must register the product under a different product code for the Rest of the World (ROW). Methods similar to the ones described below are applicable for many non-US manufacturers as well.

Learn more about the industry’s best practices, insightful recommendations, and helpful hints. Download your complimentary copy of Labeling: The Path to Global Market Clearance.

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  • Industry Reports
  • Understanding the Translation Requirements of the EU CTR
  • China Reshuffles the China Food and Drug Administration (CFDA)
  • Understanding the New IVDR
  • Why Medical Translation is a Critical Outsourced Service
  • While We Wait: The EU Joint Plan for Immediate Actions
  • The New China: Medical Device Regulatory Overhaul
  • How are the European Union Medical Device and IVD Regulations Evolving?
  • The Debate Over Changing the EU Medical Device Law
  • India’s Medical Device Market and Regulatory Landscape
  • Requirements for E-Labeling
  • ISO 14155:2011: A First Look
  • Labeling Impact on Worldwide Market Clearance
  • Directive 2007/47/EC
  • European Translation Requirements and Trends for Medical Devices and Pharmaceuticals
  • Helpful Guidelines to Choosing Your Medical Translation Partner
  • More Guidelines to Choosing Your Medical Translation Partner
  • Asian Translation Requirements – Directive 2007/47EC
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About Excel Translations

Excel Translations is a full-service, US-based corporate translation agency and technical translation agency servicing the global medical, technical, and corporate translation needs of companies and organizations worldwide.

With offices and operations in the US, Europe, and South America, we are your local and global source for translation services performed in certified quality management system ‡. If you have questions for us, you may visit our contact page.

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