We help mid-sized MedTech companies get to market faster with precise, audit-ready translations that speak the exact language of FDA, EMA, and global regulators.
At Lingrowth, we specialize in providing precise and culturally adapted translations for the medical and healthcare sectors. With a focus on compliance and innovation, we ensure your content meets the highest standards for global success.
Regulatory delays cost millions. We provide precise, audit-ready technical documentation, IFUs, and clinical data translations that pass regulatory scrutiny the first time.
63% of translation errors have clinical consequences. Your documents are localized by medical doctors and SMEs who know the strict nuances of MDR, IVDR, and FDA compliance.
You don't need a massive generalist agency. We adapt your submission strategy to each local regulator's expectations, minimizing the risk of costly deficiency letters.
Lingrowth is a medical language documentation service that helps mid-sized medical technology companies accelerate regulatory body approvals by providing subject matter experts who speak the language of regulators.
We think like reviewers. Our SMEs structure your terminology to match exactly what Notified Bodies look for, reducing questions before they arise.
A single terminological inconsistency can cause a 6-month delay. Our rigorous linguistic validation prevents clinical risks and protects your bottom line.
We integrate directly with your regulatory and development teams to localize UI/UX, Software as a Medical Device (SaMD), and hardware smoothly.
Lingrowth translation company currently provides medical translation services on the main Western European languages (English, German, French, Spanish, Italian) and Eastern European languages (Russian, Belarusian, Ukrainian, Polish, Czech, Serbian) and some Asian languages (Chinese, Japanese, Korean)
We translate the documents in the following subject matter areas: medicine, pharmaceutical, biotechnology, including patents, regulatory documents, clinical trial data,
Our support includes editing which is performed by other medical linguist who is specialized in the particular subject matter.
For your convenience, we additionally offer proofreading by a professional linguist who is a native speaker of the target language in order to check quality and style according to ISO 17100 international standard.
The client faced significant challenges in preparing documentation for a multilingual FDA submission. Their working documentation was multilingual, containing Japanese, Korean, Chinese, and English content.
Our client is a MLLSP operating in the Europe. Their core requirement is translating medical documentation across European languages. However, a significant challenge they faced was the need for direct translations between less common language pairs without using English as an intermediary
Our client is the global company specialized in medical technology and other healthcare solutions. It was founded in Ireland and operates in different corners of the world now. They innovate, advance, and implement various medical technology to make everyday life easier. The client requested a Medical App Localization service
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