Christina Miracle

Christina is a quality & regulatory affairs leader whose specialty is developing and deploying transformative solutions to improve compliance, product quality and competitive performance. She has over 15 years of medical device experience building efficient quality management systems, developing safe and effective medical devices, and gaining global market approvals.

Before joining TMRW, Christina led the global Quality Assurance and Regulatory Affairs department at Gentherm Medical where she transformed the Quality Management System to become fully compliant with all applicable global regulations. Throughout her career, she has authored many successful pre-market submissions in the top medical device markets including the US, EU, China, Japan, Australia, Canada, and Brazil, resulting in numerous safe and effective medical device launches around the world.

As the Vice President of Quality, Regulatory Affairs, and Enterprise Risk, Christina is responsible for ensuring TMRW provides safe and effective products for the management and care of frozen eggs and embryos used in IVF, leading and executing Quality, Regulatory and Enterprise Risk Management strategies and goals globally.