divendres, 13 de febrer del 2015

Regulatory affairs for medical device startups




Instilling a robust quality management system as soon as possible is crucial in becoming a successful medical device company, writes Regdy blog's Andrew Ahn.






Here's a common short-sighted view that many medical device startups have:


The 510(k) submission is the End-All-Be-All




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from MassDevice - FDA and Medical device business news and jobs for the medical device industry http://ift.tt/1zAJ29k

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