Our Medical Translation Services specialize in the translation of documents such as:
• Adverse Event Reports
• Bioequivalence Studies
• Case Report Forms (CRFs)
• Clinical Protocol/Study Synopses
• Common Technical Documents (CTDs)
• Clinical Study Reports
• Clinical Study Protocols
• Clinical Study Agreements and Contracts
• CRA Training Materials & Videos
• Source Data Sheets
• Drug Registration/Marketing Authorization Application Documentation
• GCP Documents
• GMP Documents (e.g., validation protocols/reports)
• Informed Consent Forms (ICFs)
• Instructions for Use (IFU)
• Investigator’s Brochures (IB)
• Laboratory Test Reports
• Manufacturing Process Descriptions
• Master Batch Records and Deviation Reports
• Marketing Collateral
• NDA and IND
• Package Inserts and Labels
• Patient Information
• Patient Reported Outcomes (PRO)
• Patient Recruitment Materials
• Pharmacological Studies
• Pharmacovigilance Reports
• Product Labels
• Product Licensing
• Questionnaires
• Regulatory Audit
• Regulatory Documents
• SAE and SOP
• Scientific Journal Articles
• Summary of Product Characteristics(SPC)
• Toxicology Reports
• Corporate Websites and Portals
