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Clinical Trial & research document translation



Clinical Trials Translation Services

Medical companies that are involved in clinical research and conducting clinical trials need accuracy and relevance in the translation of the clinical trials. They emphasize more on accurate content and its quality, when they engage translation services. Only when these requirements are met can the drug registration process get approval.


At iConic Translation World, we offer exemplary services to various leading medical companies specializing in clinical trials and research. We also cater to pharmaceutical companies that conduct clinical trials.


We can translate clinical research documents into over 50 global languages.


Who needs Clinical Trial document Translation service?

We proudly provide Clinical Trial document Translation service to Clinical Research Organizations(CRO), Clinical Data Management, Pharmacovigilance & Hospitals, Pharmaceutical Companies, Drug Development support services companies, Safety science companies, Safety consulting and certification company, Testing laboratories, Drug development solutions providers, Healthcare companies, global healthcare providers, Multinational pharmaceutical companies, International pharmaceutical companies, Health management companies, biotechnology companies, life sciences companies



We oversee the following documents in our services:
  • Adverse Event Source Documents
  • Case Report Forms (CRFs)
  • Clinical research
  • Data Sheets
  • Development Safety Update Reports (DSURs)
  • Dossiers
  • Drug Registration Documentation
  • Drug testing
  • Endpoint Adjudication Documents
  • Informed Consent Forms (ICFs)
  • Insert Leaflets
  • Instructions for Use (IFUs)
  • Investigator’s Brochures
  • Marketing Collateral
  • Master Batch Records
  • Medical Records
  • Package Inserts and Labels
  • Patient Diaries
  • Patient Information Sheet (PIS)
  • Patient Questionnaires
  • Patient Recruitment Materials
  • Patient Reported Outcome Measures (PROMs)
  • Patient Reported Outcomes (PROs)
  • Patient Source Documents, Admission and Discharge, Labs
  • Pharmacological Studies
  • Phases 0 - IV of clinical trials
  • Product Labels
  • Production and marketing
  • QoL Scales
  • Registration submission and review
  • Regulatory approval dossiers
  • Regulatory Documents
  • Scientific Papers
  • Study Protocols
  • Surveys
  • Suspected Unexpected Serious Adverse Reactions (SUSARs)
  • Toxicology Reports

Do you have any of the above documents to be translated?

We are here to assist you in translating them with extremely perfect quality.



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