Frank N Laban is a Pharmacist at the Zambia Medicines Regulatory Authority with 16 years of experience as a regulator in the area of medicines and medical devices regulation.

Mr. Laban is responsible for supervising marketing authorization and related activities on Medical Devices and Human Medicines and is the country focal person for the WHO PQ Collaborative Registration Procedure for In Vitro Diagnostics.

Mr. Laban has extensive experience in medical device regulation and regulatory harmonization initiatives for medical devices. During his career, he has participated in various continental activities around medical product regulatory convergence initiatives.

Frank holds a holder of a BPharm and is a candidate for MSc Pharmacy Administration and Policy