Medical Device Translations – Using Translation Memory for MDR and IVDR Compliance

Advancing Medical Device Translations with Cutting-Edge TM Technology for MDR and IVDR Compliance

In the ever-evolving global landscape of the medical device sector, the importance of precise and uniform translations has reached new heights, especially in light of the stringent regulations outlined in the Medical Devices Regulation (EU) 2017/745 (MDR) and In Vitro Diagnostic Medical Devices Regulation (EU) 2017/746 (IVDR). Against this backdrop, Translation Memory (TM) technology emerges as a paramount tool, ensuring accuracy and consistency in translations.

This article aims to illuminate the critical significance of uniformity in medical device translations and how TM technology stands as a game-changer in achieving this imperative objective.

The Imperative Need for Uniform Translations in Medical Devices

Uniformity in translations for medical devices transcends being a mere regulatory requirement; it’s a fundamental factor in safeguarding patient safety and preserving international market trust. Precise and uniform translations play a pivotal role in mitigating the risk of misinterpretation, thereby fostering a safer and more compliant global market presence for medical device companies.

Decoding Translation Memory Technology

TM technology emerges as an innovative solution for upholding uniformity in medical device translations. This technology operates by archiving previously translated source texts and their corresponding target translations, simplifying the identification and application of similar phrases in new translations. Let’s delve into how TM technology contributes to maintaining consistency:

  1. Repurposing Approved Translations: TM technology empowers the recycling of previously approved translations for new content, ensuring a consistent deployment of terminology and style across diverse documents in alignment with MDR and IVDR standards.
  2. Effective Terminology Management: TM tools play a pivotal role in creating and managing a database of standardized medical device terms, promoting lucid and compliant communication.
  3. Streamlining Updates: TM simplifies the revision process by pinpointing text segments requiring updates, guaranteeing uniform changes across all translations.
  4. Collaboration and Quality Assurance: TM fosters seamless team collaboration while upholding translation quality. Multiple translators can access the same TM database, enabling synchronized efforts supported by quality assurance features to identify and rectify linguistic inconsistencies.
  5. Customization for MDR and IVDR: Our tailored TM databases can be calibrated to meet the specific requirements of MDR and IVDR compliance. This customization encompasses the integration of regulatory terminologies and standards, further fortifying uniformity and regulatory adherence.

A Commitment to Exceptional Medical Device Translations

In the fiercely competitive realm of the medical device industry, the linchpin to success and regulatory compliance lies in the consistency of translations. By harnessing the power of TM technology, we provide medical device companies with translations that not only exemplify accuracy and uniformity but also align seamlessly with global standards and regulations. This unwavering commitment serves as a catalyst for enhancing patient safety, bolstering competitiveness, and fortifying regulatory compliance.

Our adept team at Intertranslations stands poised to assist you with our profound expertise in TM technology for your medical device translation needs. We cordially invite you to connect with us for a comprehensive discussion on how we can augment your translation requirements.

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