informedconsent – 'Femi Fajimi

May 26, 2026

Informed Consent Forms and Patient Understanding: Enhancing Accessibility from a Medical Writing Perspective

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…

Writing the Participant Information Sheet: A Practical Introduction

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…

Writing for Ethics Committee Submissions: Practical Insights from a Developing Writer

Writing for Ethics Committee Submissions: Practical Insights from a Developing Writer By ‘Femi Fajimi | May 2025 Writing for ethics committee submissions is a key responsibility in regulatory medical writing. It requires clarity, accuracy, and respect for participant rights. As I continue to build experience in this field, I understand the importance of approaching these…