Brian Goemans

Regulatory Affairs Consultant at CapeRay

Brian is a biomedical engineer with substantial experience in the development of electro-medical products, and has had considerable success in securing CE marking for medical products developed in South Africa. He worked for the Technology Innovation Agency and played a leading role in growing the medical device industry in South Africa. He assisted CapeRay to secure the CE Mark for the Pandia in 2012 and has contributed to regulatory affairs and risk management for their Aceso system. Brian consults to companies around the world through his association with Emergo, a global medical device regulatory consultancy. He has a BSc in Electrical Engineering from Wits University and an MSc in Biomedical Engineering from UCT.

Timeline

  • Regulatory Affairs Consultant

    Current role