Dr. Shellan Omondi is a Regulatory Officer at the Pharmacy and Poisons Board (PPB) of Kenya, working in the Medical Devices and In Vitro Diagnostics (IVD) Unit of the Department of Product Evaluation and Registration.

He is actively involved in the assessment, regulation, and oversight of medical devices and IVDs to ensure their safety, quality, and performance, while also contributing to the development of regulatory frameworks that strengthen systems, align with global standards, and promote regional harmonization.

His work spans device registration, post-market surveillance, reliance models, and addressing emerging challenges such as digital health, traceability, and counterfeits, with a strong focus on building resilient and patient-centered regulatory ecosystems.