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.
iConic Translation World is an ISO Certified company and we are a global translation service provider that provides solutions to various industry sectors all over world.
Having Registered office at Chennai, Head office at Goa, We have our branch offices in Bangalore, Hyderabad, Mumbai & Malaysia.
Most Competitive Price:
We offer the most competitive price that fits your budget. We charge a very reasonable & affordable price which starts from just $0.04/₹1.50 per word.
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)
Development Safety Update Reports (DSURs)
Drug Registration Documentation
Endpoint Adjudication Documents
Informed Consent Forms (ICFs)
Instructions for Use (IFUs)
Master Batch Records
Package Inserts and Labels
Patient Information Sheet (PIS)
Patient Recruitment Materials
Patient Reported Outcome Measures (PROMs)
Patient Reported Outcomes (PROs)
Patient Source Documents, Admission and Discharge, Labs
Phases 0 - IV of clinical trials
Production and marketing
Registration submission and review
Regulatory approval dossiers
Suspected Unexpected Serious Adverse Reactions (SUSARs)
Do you have any of the above documents to be translated? We are here to assist you in translating them with extremely perfect quality. All you need to do is, write to us or Request a free Quotation along with the document(s) to be translated.
E-mail id: email@example.com
For any queries, Please call +917066154586