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It’s your job to develop the life-saving drug therapies and medical devices that make the world a healthier place. Let us be your trusted partner for regulated, compliant life science translations and linguistic validation, as well as advanced multimedia and marketing services designed for life sciences. From IP protection to clinical trials, drug filings to product launches, our propositions build on advanced translation methodologies to enable the safe use of your products and support the full life cycle of your drugs and devices. All with the accuracy you require to bring your messages and products to the world—safely, accurately, efficiently, and in regulatory compliance.
At every touchpoint on your go-to-market journey, from drug or device development to the moment your product makes its way safely and effectively to patients worldwide, Lionbridge helps you get there faster—with less risk.
Get to know your compliance partners
Lead the way with high-quality, compliant global clinical trial translations from the very beginning. A strong start is critical for an effective clinical trial. Consider language translation from the beginning, and you’ll realize a stronger trial execution—from study start-up to study report. Global clinical trial planning requires early and sophisticated consideration of the costs, complexities, and risks surrounding communications. Language is a mission—critical element of culturally and regulatory appropriate content containing all forms of communication.
Lionbridge Life Sciences has extensive experience in global clinical trial translation, providing end—to—end services for a wide range of documentation. Our clinical teams scale programs for trials of all sizes, offering service and support on a global scale to produce accurate, consistent translations and deliver the greatest impact for your message across many languages, markets, and cultures.
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.
Gary Abernathy
Executive Director, Supply Chain, Karyopharm