My name is Ebrahim Njar and I am the global regulatory affairs specialist at BioScience GmbH. I graduated from Ajman University with a Bachelor of Science in Biomedical Engineering in late 2017, and have been working in the medical device regulatory affairs industry since 2018 with a main focus on MDs regulations in the MENA region. I also possess a strong understanding of the new European medical device regulations 2017/745 (MDR) and their implications on our regional regulations. I am an IRCA certified auditor for both ISO 13485 (medical devices quality management systems) and ISO 9001 (quality management systems). I am currently finishing my Master of Science program at Arizona State University with a major in Clinical Research Management and a minor in Regulatory Science.