Whether it’s medical devices, pharma, clinical research, or healthcare, our life science translation experts are constantly adapting and evolving with the industry.
Foreign markets present enormous growth opportunities for medical device manufacturers. But in their efforts to go global, companies need to remain compliant with international and local regulations in each country. We help ensure your products reach new markets and comply with all regulatory and cultural requirements through every stage of the product lifecycle.
The number of clinical trials conducted internationally keeps growing every year and that is why translation has become a fundamental step throughout clinical trial processes. We translate all kinds of clinical trial documents, from patient questionnaires to case report forms. As an ISO 9001 certified provider, we consistently deliver linguistically accurate, culturally localized documents for the intended target audience whether its physicians, patients, or review boards.
Translations are usually required at several stages during the process of developing a new drug and its commercialization across international markets — clinical research, regulatory submissions, label and packaging as well as marketing & commercialization. We support leading pharmaceutical and biotech companies with 360° language solutions that comply with all local regulatory requirements and help deliver reliable outcomes to patients worldwide.
Healthcare organizations such as hospitals, nursing homes, and rehabilitation centers face constant pressure to guarantee increased access and smoother patient experiences. At Yelllow Hub, we believe language barriers should never be an obstacle to providing quality healthcare. Our team of specialized medical translators helps leading healthcare organizations to deliver seamless patient experiences in any language.
We understand the need to stay current in an increasingly regulated industry like life science. That’s why we keep a close watch on the evolving linguistic validation methodologies and other regulations by entities such as the American Food and Drug Administration Agency (FDA) and European Union guidelines) with a focus on global patients.
You can rely on our dedicated account managers to handle any questions you may have and keep you updated with the progress of your projects.
We recognize the value of data security and confidentiality when it comes to legal documents and deems all disclosed data, ideas, and all sources of oral and written information to be strictly confidential.
We are accredited to ISO 9001 for quality systems and ISO 17100, which covers all aspects of the translation process directly affecting the quality and delivery of translation services.