Delays or errors in regulatory or clinical documents can jeopardize approvals, compliance, and patient safety. That’s why precise, expert translation is not optional—it’s critical. 

With over 20 years of experience in the translation of regulatory and clinical documentation, I provide precise, reliable, and fully compliant translations for pharmaceutical companies, CROs, and medical device manufacturers. My work spans informed consent forms, clinical trial protocols, instructions for use (IFU), summaries of product characteristics (SMPC), packaging materials, regulatory submissions, and all types of scientific and promotional documentation. I combine linguistic expertise with a deep understanding of regulatory frameworks, including Drug Regulatory Affairs, ICH E6, and other international guidelines, ensuring your materials meet both legal and practical requirements. 

I specialize in plain language, making complex medical, legal, and technical content accessible to professionals, patients, and broader audiences without compromising scientific accuracy. I deliver translations that support compliance, clarity, and successful communication across Spanish-speaking markets.