Profile Summary Multilingual regulatory translator with over twenty years of experience in technical and compliance documentation. I specialize in pharmaceutical, medical device, technical, industrial, and legal translation, where precision and regulatory compliance are paramount. Following three years of collaboration with Kazakhstan’s pharmaceutical and medical device authorities, I have developed a solid understanding of both EU (EMA/ICH/MDR/IVDR) and Kazakhstan NDDA frameworks. My translation work bridges these regulatory environments, covering submission dossiers, pharmacovigilance materials, and labelling, to ensure that every document is linguistically accurate and fully compliant with market access requirements. Key fields: regulatory affairs, clinical and technical documentation, procurement and supply chain materials, and market-entry communication. Languages: English, Italian, Russian, and Kazakh. Objective: to provide precise, audit-ready translations that support safe product registration and foster transparent international communication. Education │ CPD Courses │ Legal Status - Pharmaceutical Supply Management for LMI Countries (Udemy) - Clinical Trials and Medical Documentation (ProZ.com) - The Medical Translator’s First Aid Kit (ProZ.com) - Master’s Degree in International Trade – Italy - Bachelor’s Degree in Translation and Interpretation – Kazakhstan EU work authorization (Italian citizenship)