We handle all types of clinical research documents, from contracts and informed consent forms to protocols and study reports across different research phases. Our primary focus is ensuring precision, regulatory compliance, and clarity in every delivery.

We translate administrative documents, training materials, patient guidelines, and clinical directives. For each project, we carefully assess the target audience, adapting language to the context of each material, balancing accessibility, clarity, and terminological precision.

We understand the requirements set by regulatory bodies such as ANVISA, FDA, and EMA. Our translations strictly follow regulatory guidelines, supporting the market entry of new technologies. We translate drug registration dossiers, clinical reports, and other critical documents with precision and clarity.

Bringing new medical technologies to market demands clear, technically accurate, and consistent translations. We have experience translating instructions for use (IFUs), safety manuals, and registration dossiers.

We translate drug dossiers, package inserts, and pharmacovigilance reports with meticulous attention to industry-specific terminology. Our goal is to ensure complex information is communicated accurately and consistently, adhering to regulatory standards and maintaining clarity for each audience.

We provide translations for comprehensive 360º marketing strategies, both online and offline. Our expertise covers promotional and non-promotional materials, medical e-learning content, and health-awareness campaigns, all aligned with regulatory standards