Salim Khan is a highly experienced Medical Device Risk Management and Quality Management Systems Consultant with over 20 years in the medical device industry. He brings extensive expertise in implementing design control processes, risk management, and quality systems that comply with regulatory requirements and international standards, including ISO 13485 and ISO 14971. Throughout his career, Salim has played a key role in new product development, as well as managing post-production activities such as non-conformance investigations, CAPA, complaint trending, and problem-solving. His deep knowledge and experience ensure that companies meet regulatory standards while maintaining high-quality product outcomes.
