With years of industry experience, MedEdge offers valuable insights into strategic and investment planning. We can also serve various roles on a day-to-day basis from project manager for development of new technologies, or a critical team member working closely with R&D and manufacturing engineers. We offer training and management of necessary but often overlooked areas of quality and design history file requirements to ensure no aspect is overlooked during the product development process.
Regulatory Affairs | Quality Systems and Compliance Clinical Trials with Device Support | Global Health
A boutique consulting firm offering customized services to medical device, diagnostic, and pharmaceutical companies.
Focus areas include: Regulatory Affairs, Quality Systems and Compliance, Clinical Trials with Device Support, and Global Health.
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