Life-sciences products move across countries, languages, and regulatory environments making accurate translation essential from development to market. Avanteva supports global clinical trials, manufacturing, packaging, and regulatory submissions with certified language specialists who understand scientific and regulatory terminology.
Our native expert translators ensure clarity, consistency, and preservation of meaning across clinical and non-clinical documents, delivered reliably within committed timelines.
Clinical Trial Documents
Informed consent forms, study protocols, and patient information leaflets translated with regulatory precision
Safety Reporting
Pharmacovigilance reports and adverse event documentation in multiple languages
Medical Device Materials
User manuals, technical specifications, and device labeling for global markets
Patient Materials
Patient diaries, questionnaires, and educational materials ensuring cultural appropriateness
Why Avanteva
Certified domain-expert translators
Clinical & regulatory terminology expertise
Consistent, audit-ready quality
Reliable turnaround times
Partner With Avanteva Today !
Contact our team to discuss how we can support your compliance objectives and accelerate your regulatory readiness.
