Q BioMed Inc. announced the appointment of Geoff Fatzinger as the Global Head of Regulatory Affairs. Geoff will be responsible for providing strategic regulatory oversight to Q BioMed for product development and commercialization. Specifically, he will be focused on developing the global regulatory approval strategy for the commercialization of Q BioMed's lead product, the FDA approved, non-opioid Strontium89 (Strontium Chloride Sr-89 Injection, USP). He will also contribute strategic regulatory insight and guidance to the Company's portfolio of earlier stage assets. Geoff brings over 20 years of regulatory expertise, having been directly involved in all phases of product development with a demonstrated record of regulatory and business accomplishments covering the United States, Europe, Middle East and Asia Pacific with in-depth experience in Japan, China, and Korea.