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Concordis Language Services provides professional clinical protocol translation services in over 100 languages, and continues to expand into other languages as the importance of clinical protocol and research grows in other parts of the world. Our knowledgeable and expert translators who are trained in translating clinical trial documents for various clinical research organizations and pharmaceutical companies can help you get maneuver through the regulatory process on national and international markets. 

What is a Clinical Protocol?

In natural sciences, a clinical protocol is a document that describes in what manner a clinical trial will be carried out, including its design, methodologies, objective, and statistical considerations. Its main objectives are to maintain the safety of the trial subjects as well as to ensure and safeguard the quality and integrity of the data collected.

Clinical Protocol Documents We Translate

  • Adverse Event Reports

  • Case Report Forms (CRFs)

  • Clinical Outcome Assessment

  • Clinical Protocols

  • Doctor and Patient Guides

  • Drug Inserts

  • Drug Study Labels

  • ​Ethics Correspondence

  • Event Logs

  • Informed Consent Forms (ICF)

  • Instructions for Use (IFUs)

  • Investigator's Brochures (IB)

  • Master Batch Records

  • Patient Diaries

  • Patient Information Leaflets (PIL)

  • Patient Questionnaires

  • Patient Records

  • Patient-Reported Outcomes (PROs)

  • Pharmacological Studies

  • Protocol Synopsis

  • Regulatory Documents

  • Study Protocols

How to contact us

For more information about our Clinical Protocol Translation Services, please contact us by sending an e-mail to or by calling (413) 345-2587 or (332) 203-7018.

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