The FDA has changed the way it views Cybersecurity in regards to premarket submissions for medical devices.
Federal standards governing the safety and efficacy of medical products have been overseen in the United States by the FDA since t...
In the medical device industry, every company knows the necessity of a Quality Management System (QMS) for managing internal proce...
Regardless of industry, any company writing code understands the need for standardization and proof-checking, and the medical devi...
What is The MC2? The MC2 is a new tool designed to level-set expectations and aid contract negotiations for medical device purchas...
Velentium, a professional engineering firm that specializes in the design and manufacturing of therapeutic and diagnostic active m...
In "28 Days to Save the World," he lays out how to harness the power of organizational culture to prepare your small business to w...
One Stop for Medical Device R&D, Product Development, Contract Manufacturing, and Postmarket..
