Rania Ibrahim

Regulatory Affairs Leader, Clinical Trials Expert,  GMP & Pharmacovigilance Strategist. With over 20 years of experience in pharmaceutical regulation, clinical trials oversight, and biomanufacturing, I currently lead the General Administration of Clinical Trials at the Egyptian Drug Authority (EDA). My work spans GCP inspections, regulatory strategy, and scientific committee coordination for biological and innovative products.

I’m passionate about strengthening global clinical trial ecosystems and actively contribute to international regulatory forums including WHO’s Global Clinical Trials Forum, ICMRA, and AVAREF. I also lecture at King’s College London, sharing insights on drug regulatory affairs.

My background includes leadership roles in GMP inspection, pharmacovigilance, and operations management, with certifications in ISO 9001:2015 auditing, healthcare quality, and clinical trial protocol assessment. I’ve presented at global conferences and collaborated with WHO, AUDA-NEPAD, and other institutions to advance regulatory science across Africa and beyond.

Fluent in Arabic and English | Working knowledge of French Based in Cairo, Egypt | Open to global collaboration.