About me
Madiha is a pharmaceutical industry professional with a background in fundamental bench research. Her experience as a regulatory medical writer working with small, mid-size, and large pharmaceutical companies over the past 10 years has given her an in-depth understanding of all phases of drug development, from discovery to post-authorization. Her areas of expertise include IND/NDA/BLA submissions, development of clinical protocols, briefing documents for health authority interactions, and program management. She holds a PhD and BSc in Chemistry (double minors: Applied Statistics, Psychology), with 3 years of postdoctoral experience in Pharmacology/Toxicology.
