Cheryl Tal

Ms. Tal has over 20 years of experience in regulatory affairs, quality assurance and clinical trials for the medical device and pharmaceutical industry.  She has established and implemented quality management systems, obtained worldwide regulatory licenses and handled clinical trials for a wide variety of medical devices in all stages of development.  Her experience covers both start-up and large global companies, including managing QA/RA teams and CRO’s.

Ms. Tal has worked in the past in various managerial positions at Redent Nova, Change Healthcare and New Phase.