Excel Translations

Excellence for Global Growth

Offices and Operation Centers
in North America, Europe, and South America
  • Medical
  • Technical
  • Corporate
  • Processes
  • Certifications
  • Services
  • Contact
  • Blog
  • Industry Reports

Requirements for E-Labeling

e-labelingThe technological benefits of e-labeling are recognized by the European Union; however, having labeling available in electronic formats cannot be achieved without some serious considerations. Throughout the course of our day we may frequently create and distribute electronic copies of documents as if it were second nature. The process of creating electronic copies of labeling is not as simple as merely generating an Adobe PDF document

The draft regulation sent to the WTO for adoption has specific guidelines regarding what types of medical devices can use e-labeling, what types of documents can be available in an electronic format, and what types of steps must be taken to mitigate risk. A copy of this draft regulation is available for download along with the summary of these guidelines presented in a report that is available for free download.

Download your complementary article: “Requirements for e-Labeling” now and learn what is required and what you must consider when you choose to make you labeling available in electronic format.

Download
Excel Translations Overview
Learn how the new EU Clinical Trials Regulation 536/2014 (CTR) may impact your translation processes

For a FREE Translation Quote

Name*
GDPR Agreement*
This field is for validation purposes and should be left unchanged.

  • 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
  • Best practices for your Translations Memories

Search

 

 

Excel Translations Overview

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.

Connect With Us

  • Facebook
  • LinkedIn
  • Twitter

View our Privacy Policy

© 2025 · Excel Translations

We use cookies to ensure that we give you the best experience on our website. If you continue to use this site we will assume that you are happy with it.OkPrivacy policy

Notifications