Melissa Masters is the president of CMD MedTech. Ms. Masters is a medical device development expert and has more than 18 years of experience in product development as a project manager, systems engineer and design engineer, serving as the project manager and lead systems engineer on medical device development and sustaining engineering programs. Capabilities include leading a large multi-disciplinary team, leading risk assessments, creation of design inputs, design, specification creation, design verification, task management and conducting clinical trials involving human subjects.
She has been published and widely quoted on a variety of medical device and medical cybersecurity topics in AAMI Horizons, Journal of mHealth, Medical Products Outsourcing, Mass Device, ExecutiveGov.com, and Fierce Medical Devices. She has also participated in podium talks and panel discussions for Advamed, INCOSE, MD&M West, BioOhio, HBA and the HIMSS Privacy and Security Forum.
In addition, Ms. Masters holds a Regulatory Affairs Certification (RAC) and has a working knowledge of domestic and international regulatory requirements for medical devices.
