Catherine Bruno Undiri is a licensed pharmacist with experience in pharmaceutical regulation, quality assurance, pharmacovigilance, and medical devices regulation. She has worked extensively in regulatory compliance, clinical trial assessment, product registration, and quality systems for medicines and medical devices.

She currently serves as a Regulatory Affairs Officer at Japan Tanzania Medical Instrument Company Ltd (JTMI), overseeing regulatory compliance and medical device operations. She has also worked as an External Expert Assessor and Intern Pharmacist at TMDA, supporting clinical trial reviews, pharmacovigilance activities, and product registration processes.