Case Study: Leading Pharmaceutical Company achieves on-time EU-CTR submissions with IQVIA Language Solutions

Delivering translated 30+ informed patient consent forms (ICFs) for 13 countries, ahead of timelines

Leading Pharmaceutical Company faced tight EU Clinical Trials Regulation (EU‑CTR) deadlines and complex local language requirements for informed consent forms (ICFs), where translation delays or errors could jeopardize regulatory approval. They engaged IQVIA (IQVIA Language Solutions) to ensure timely, accurate, and patient‑centric translations across multiple member states.

IQVIA deployed a regulatory‑focused language solutions framework—including layperson translations, rigorous quality controls, and close client communication—and translated 30+ ICFs into 13 languages in under 8 days, ahead of the deadline. IQVIA’s work enabled timely approvals, improved patient understanding and safety, and boosted operational efficiency for the trial.