Senior regulatory expert with over 20 years of experience within the Tunisian National Regulatory Authority (NRA), specializing in the evaluation and regulation of medical products, including biologics, vaccines, biosimilars, and pharmaceuticals. Extensive experience in CMC assessment, pharmacology and toxicology, GMP inspections, and regulatory system strengthening. Actively engaged in WHO initiatives, including ECBS, CRP, and Global Benchmarking Tool (GBT) processes, with strong involvement in regional harmonization (NA-MRH) and reliance-based regulatory frameworks.