Informed Consent Form Review

Informed Consent Forms (ICFs) serve as critical components in the conduct of clinical trials, with privacy considerations now playing a central role in these documents. Ensuring that ICFs are meticulously reviewed is essential for securing clinical trial authorization; this involves incorporating appropriate language that aligns with European regulatory requirements, while also considering national and regional prerequisites. Such attention to detail in the preparation of ICFs can help to preempt and avoid potential objections from Ethical Committees. Drawing on its extensive experience across the EU, iliomad is well-positioned to expedite this process effectively.