Mary Beth McDonald

Vp, Regulatory And Quality Management at Glooko

Mary Beth McDonald possesses extensive experience in regulatory and quality management within the medical device and pharmaceutical industries. Currently serving as VP of Regulatory and Quality Management at Glooko, Mary Beth has previously held significant roles, including Sr. Director of Quality Assurance at Chrono Therapeutics and Alexza Pharmaceuticals, and Director of Quality Systems at Scanadu. In addition to industry roles, Mary Beth contributes to academia as an instructor for the Medical Device Certificate Program at UCSC Silicon Valley.

Location

San Francisco, United States

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Glooko

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Glooko is transforming digital health by connecting people with diabetes and related conditions and their healthcare professionals, enabling telehealth, clinical research, and improved collaboration. The company’s software platforms empower the management of diabetes and other chronic conditions by collecting and unlocking the power of data from blood-glucose meters, CGMs, insulin pumps, connected insulin pens, wearables, connected scales, blood pressure cuffs and activity trackers – bringing insights together in one place.


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Employees

51-200

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