As medical device technology continues to advance on a global scale, regulations within the industry advance at the same rate, generating a roadblock to success: Labeling translation. Medical translation services deliver absolute precision, with rigid adherence to deadlines, costs, cultural sensitivity – and quality you can trust. Lionbridge Life Sciences provides industry-leading expertise, enabling you to seamlessly manage global regulatory risk, improve communication with physicians and keep pace with the constantly accelerating medical device world.
Make high-quality translation a high priority
International regulations require medical device companies to localize labeling – including software, user manuals, instructions for use (IFU) and labels – into an ever-increasing number of languages. (The average is as high as 22 languages.) Our global experts have deep knowledge of medical device translation, from initial product submissions to production-ready labeling, and we’re ready to help your company.
When you partner with Lionbridge Life Sciences, you’ll work with a dedicated team well versed in the unique challenges of life sciences. With over 40 full-scale Solution Centers that span 26 countries, we can quickly scale programs to meet your medical device labeling needs worldwide.
Lionbridge Life Sciences can help you reach your worldwide localization goals through:
- High-quality labeling and packaging
We provide a range of services, including artwork preparation (label, secondary packaging components), Structured Product Labeling (SPL), labeling updates and amendments, Product Information Leaflets (PIL), patient handbooks, data sheets, user guides, technical manuals and software.
- ISO certifications and rigorous quality methodologies
We strictly adhere to methodologies designed specifically for medical device labeling and applied across our specialized Life Science Centers of Excellence.
- Software expertise
We streamline localization by helping define and drive software development, then performing UI translation, engineering and testing for any language, in any country.
- Innovative technology
We stay a step ahead with SaaS-based tools for project submission, linguistic asset management and reporting that can improve cost efficiencies and accelerate timelines.
- Auditable processes
We tailor our standardized, company-wide processes to the medical device industry.
- Cloud-based content
We share and re-use translated electronic content from prior studies through our safe and convenient Translation Memory in the Cloud.
- Data collection best practices
We can apply the data collection best practices we’ve developed from years of working in emerging markets – all to help you comply with worldwide regulations, as well as guidance for data quality and integrity traceability.
Our team ensures global interoperability of medical device software by offering solutions for:
- User interfaces (UI)
- Software applications
- Online learning content
- Online help