Ms. Khatija Suleman is an accomplished healthcare professional with over 30 years of experience in regulatory affairs, clinical pharmacology, and medical device industries. She currently serves as a member of the SAMED (South African Medical Device Industry) board and represents the organization at key industry events.

Throughout her career, Khatija has held various roles within regulatory affairs, medical affairs, pharmacovigilance, and quality management, with a strong focus on ensuring the safety, compliance, and effective use of healthcare products. Her deep expertise spans regulatory strategy, compliance frameworks, and clinical trials, allowing her to effectively navigate complex regulatory environments and deliver impactful solutions for the medical and pharmaceutical industries.

Ms. Khatija is known for her ability to quickly adapt to new challenges, lead cross-functional teams, and implement strategies that drive operational excellence. She has worked in both local and international settings, gaining valuable experience in multicultural environments that have enhanced her regulatory insight and approach to global healthcare standards.