Linguistic Services: Translation, Review, and Patient Adaptation

Linguistic consultancy for the pharmaceutical sector, biomedical research, CROs, biotech, and health communication.

20 years of communicating science with precision.

Linguist specializing in scientific articles, clinical trials, and regulatory documentation for researchers, CROs, and healthcare sector entities.

They trust us

How can I help you?

Specialized services for every stage of your research and scientific documentation.

traductor español inglés traductor de artículos

Scientific Article Translation

Translation of manuscripts, scientific papers, and systematic reviews with rigorous terminology management and adaptation to the editorial standards of leading biomedical journals. Proven results: clients with successful publication in Q1 and Q2 journals.

Científico revisando un manuscrito en su ordenador, mostrando la importancia de publicar artículos científicos

Clinical Trial Documentation

Protocols, ICFs, eCRFs, safety reports, and documentation for CROs. In-depth knowledge of GCP, EMA, FDA, AEMPS, and ICH guidelines. Absolute confidentiality guaranteed.

traductor de artículos, revisor de artículos, traducción de papers, traducción de manuscritos

Translation for Biotech Companies and Science & Technology Parks

Comprehensive coverage across the entire product lifecycle: SmPCs, labeling, patents, regulatory dossiers, and R&D reports. Integrated translation services for companies based in science and technology parks, innovation hubs, and biotech ecosystems.

Your research, in the language of success.

More than 1,000 articles translated and published in international journals. A specialist with in-depth knowledge of the entire scientific publishing process.

Terminological Precision

More than 1,000 articles published in high-impact international journals stand behind every project. Impeccable biomedical terminology, strict adherence to editorial style conventions, and native-level fluency in both English and Spanish.

Regulatory compliance

In-depth knowledge of the regulations governing clinical trials and pharmaceutical documentation. Your regulatory documents will be accurate, confidential, and ready for submission to any regulatory authority.

Personalized and confidencial service

Work directly with Nuria—no intermediaries or automated platforms. Personalized guidance included: journal selection, adaptation to editorial style requirements, and support in responding to reviewers’ comments.

Let´s talk about your project

Do you have a manuscript, protocol, or file that needs translating or reviewing? Write to us and we’ll give you a quote within 24 hours, with no obligation.

Name

Email

proyectos@traductorescientificos.es

Phone and Whatsapp

+34 687 98 80 96