IQVIA Clinical Trials Localization

When Global Trials Meet Local Requirements

Scale across languages and regions with IQVIA Clinical Trials Localization

IQVIA Language Solutions

Successfully navigate pre-clinical regulatory requirements

In the pre-clinical phase, accurate documentation is vital for regulatory submissions and study approvals. Our team can assist with:

  • Protocol Translations: Ensuring study protocols meet regulatory requirements across regions.
  • Investigator Brochures: Providing precise translations for investigators.
  • Ethics Committee Correspondence: Facilitating clear communication to obtain approvals and address concerns.

IQVIA Language Solutions

Execute your global clinical trials with precision

While providing reliable language accuracy and the highest level of security and compliance, our life sciences solutions to are designed to help you overcome language, cultural, and accessibility barriers in clinical trials while accelerating patients access to innovative medicines.
25%

Reducing cost of clinical translation Project delivered for a top pharma client

300%

more stringent quality indices compared to legacy language models

14,000

Informed Consent Forms and Protocols Translated in 2024

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