John Mann
VP Quality Assurance and Regulatory Affairs
With 30 years of experience in the medical device industry, John specializes in regulatory affairs and quality management systems. He has led the integration and execution of regulatory approvals for various class devices in the USA and EU, mitigated recalls, and designed compliant QMS for global regulations. John has expertise in FDA QSR, ISO13485:2016, ISO9001:2015, and other key standards, providing practical compliance solutions. He is known for his leadership and presentations in the field.