MedEdge
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MedEdge
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At MedEdge, we understand that time is money. That’s why we provide guidance and resources to obtain high quality objectives in an efficient manner to reduce time to market while maintaining safety and regulatory compliance.

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About Us

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. 


Our Focus Areas

Regulatory Affairs | Quality Systems and Compliance Clinical Trials with Device Support | Global Health

We are proud to have partnered with over 50 companies in the last 10 years to complete clinical trials, obtain ISO certification, and gain US, European, and global commercial clearance for products.

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MedEdge

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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