Ms. Thomas has over 15 years of experience in the medical industry. She has guided companies through the medical device regulatory maze to successfully register and launch products globally. She initially worked as a product development engineer and then transitioned to the Regulatory Affairs department. She has her RAC (Regulatory Affairs Certification) professional credential from the Regulatory Affairs Professional Society. Her medical product experience ranges from research on novel devices, to orthopedic implants, jet injection devices, orthodontic devices, and more. Alyssa is currently the principal consultant at Allegiance Regulatory Consulting LLC. Prior to her work in the medical industry, Alyssa worked as a process engineer, engineering manager and supplier quality engineer in the high-tech industry.
Alyssa can provide advice and assistance on regulatory strategy planning, global new product registration submissions, compliant quality management systems, regulatory authority interactions, compliant product labeling and interpretation of global standards, guidance documents and regulations. She can provide guidance on compliant product development activities that will allow companies to efficiently navigate the regulatory maze in order to launch products and generate revenue quickly.