Compliance with Good Clinical Practice (GCP)

🌍 Languages We Support in Clinical Trials

Multilingual Patient Recruitment & Communication

• Assist with identifying, pre-screening, and enrolling participants across multiple languages

• Provide interpretation or translation during the informed consent process (ICF)

• Facilitate culturally sensitive patient communication to support retention and compliance

• Support follow-up visits and calls with language-accurate messaging

Clinical Trials Data Entry & Adverse Event (AE) Narrative Translation

• Translate and verify AE narratives in compliance with study protocols and global safety reporting standards

• Collect AE data during remote calls and input it into EDC platforms (e.g., Medidata, Oracle, Veeva)

• Support narrative accuracy by reviewing and translating foreign-language responses into English

• Assist in structured eCRF data entry and multilingual quality control in CRDM systems

🌐 🇩🇪 German

🌐🇫🇷 French

🌐 🇪🇸 Spanish

🌐 🇺🇸 English

🌐 UK English

🌐 🇨🇳 Chinese (Mandarin)