Helping you contribute to safer medicine everywhere
We eliminate communication barriers, so you can speak clearly to patients and healthcare professionals all over the world.
It’s your job to develop the life-saving drugs and devices that make the world a healthier place. Let us be your trusted partner. From IP protection to clinical trials to supporting the safe use of your products, we help you with the details and deliverables you need to bring your messages and products to the world—safely, accurately, efficiently, and in regulatory compliance.
“[Lionbridge] really adapted to our needs. They understood what we were looking for, and they came to the table with some very unique and appropriate solutions to address our needs.”
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Bring your drugs to market as quickly as possible, so you can deliver medicine safely and effectively to the people who need it most around the world.
Accurate and compliant regulatory drug labels are critical elements of an expedient go-to-market strategy. Regulatory compliance, accurate translation, and the correct use of standardized medical terminology, such as MedDRA and EDQM, facilitate correct drug administration, irrespective of the market or therapeutic indication.
What’s more, global product launches often require translations into an overwhelming number of languages and layers of regulations with which to comply.
To ensure accuracy and compliance without sacrificing speed, you need a qualified Language Services Provider. You need Lionbridge.
Get started today—contact us and speak with an expert to learn how we can ensure accurate, compliant translations for your all-important clinical trials.