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Life sciences and medical translation services

Regulatory developments, shifting expectations, and constant innovation all require technically precise, consistent and high-quality translated content. As a trusted medical translation provider, we understand the challenges faced by the constantly evolving medical industry.

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Trusted medical translation service

LanguageWire has a deep understanding of the life sciences industry and medical translation requirements. You can trust us with your SOPs, the creation of content workflows tailored to your needs, and streamlined collaboration with expert medical translators.

Whether you are a biotech firm, clinical research organisation, pharmaceutical company or a manufacturer of medical devices, we are ready to take your content global.

We handle a wide range of life sciences
and medical translations

We understand that you need technically precise, consistent, and high-quality documentation for every phase of your operations – from research and development to submissions for regulatory review and approval, commercialisation and marketing.

Clinical trial protocols and safety reports

Instructions for use (IFU) of medical devices

Marketing content

Package inserts and labelling

Patient information leaflets

Standard operating procedures (SOP)

ISO 13485 medical devices certified

Learn about our ISO credentials; security management, translation workflows, post-editing MT, and quality management. We’re also ISO 13485 Medical Devices compliant and have proven experience with the following regulatory and risk management standards:

  • Compliance with European Union Directives
  • ISO 13485 Medical Devices – Quality Management
  • Risk management for labelling and documentation
  • Translation services for CE Mark and FDA requirements.
Regulatory affairs

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What differentiates LanguageWire is speed and value. Not only are they very responsive to our fast-changing requirements, but they are able to guide us through new processes and help us to gain efficiencies continuously.

Global Marketing Manager,


LanguageWire ecosystem & life sciences

Our ecosystem supports your medical content needs in one place. Combining advanced AI and industry experts, we offer quality technical writing solutions to service the full range of medical content.

Clinical trial translations

Since 2001, we’ve provided clinical trial documentation translations to sponsors (pharmaceutical, biotech and medical device clients) and clinical research organisations (CROs).

  • Informed consent forms (ICFs)
  • Patient questionnaires
  • Adverse event forms / reports
  • eDiaries / event logs
  • Protocols
  • Patient diaries
  • PRO / ePRO
  • eCRF / CRF

Medical devices translations

Translations for medical devices require accuracy, usability, and more accuracy. Enjoy peace-of-mind thanks to fully compliant translations.

  • User guides and manuals
  • Packaging
  • Instructions for use (IFU)
  • Development safety update reports
  • Patents for medical and surgical devices
  • Software applications and documentation
  • Package inserts and labels
Clinical trials

Regulatory affairs

Meeting product information requirements is essential. Many of the world’s leading pharmaceutical organisations benefit from the built-in MedDRA and EDQM dictionaries in our Translation Memories for centralised, mutual recognition and decentralised procedures.

  • Patient information leaflets (PILs)
  • Inserts / prescription information
  • Product information
  • Summary of product characteristics (SmPCs)
  • Correspondence for any side effects

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How can we help you?

Your journey to a powerful, seamless language management experience starts here! Tell us about your needs and we will tailor the perfect solution to your enterprise.