Case Study
Ensuring Timely and Accurate EU-CTR Submissions
Delivering translated 30+ informed patient consent forms (ICFs) for 13 countries, ahead of timelines
May 23, 2025
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As part of the EU Clinical Trials Regulation (EU CTR), a leading pharmaceutical company needed timely submission of Informed Consent Forms (ICFs) to ensure regulatory approval. IQVIA managed the translation of 30+ ICFs into 13 languages within 8 days, delivering ahead of the deadline.

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