Iris Diagnostics, Inc. is a global consultancy and training firm focused on in vitro and medical device regulatory compliance, quality management, auditing, and training for US and international regulations. Formerly RM Clinical Consulting, Iris Diagnostics was formed in 2019 as a group of industry professionals seeking to work together and provide prospective clients with a complete set of solutions. Industry and governmental clients have come to trust us for our deep subject matter expertise and proven ability to deliver long-term results. Our fluency in regulatory requirements and improvement methodologies allows our customers to boost performance while safeguarding or improving their regulatory compliance.