ICF
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An educational narrative review from a medical writing perspective By Femi Fajimi | 26 May 2026 Abstract Informed consent forms (ICFs) are foundational to ethical clinical research, designed to protect voluntary participation and autonomous decision-making. However, modern ICFs have evolved into lengthy, dense documents filled with complex scientific, legal, and regulatory terminology that vastly exceed…
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Writing the Participant Information Sheet: A Practical Introduction By ‘Femi Fajimi | 15 May 2025 The Participant Information Sheet (PIS) is one of the most important documents a medical writer may help prepare during the early phases of a clinical trial. In plain and respectful language, it explains what the study is about, what participation…