informedconsent
-
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 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
'Femi Fajimi 