Clinical Trial Related Documents

TOIN provides language support for all applications and paperworks required by pharmaceutical manufacturers including clinical trials and trial related documents as well as translation of application forms and other materials. Based on the knowledge cultivated from the many years of translation support provided to foreign manufacturers, TOIN can provide high-quality translations that accurately grasps the context with the correct terminology and phrases.

Languages
Deliverables
Investigational Drug Summary Clinical Trial Plan (Protocol) Case Report Overall Report Suspect Adverse Reaction Report (CIOMS Form, etc.) Application Related Document (IND, NDA, ANDA, etc.) Post-Marketing Safety Report (PSUR, etc.) Chemistry, Manufacturing and Controls (CMC) Material Safety Data Sheet (MSDS) FDA, EMA Documents (CTD etc.) Other Clinical Trial Documents
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