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Robert van Boxtel has over 20 years of experience in the medical device industry, working first in medical device production sites in the Netherlands and USA, and later on worked for the Dutch Notified Body KEMA Quality (now Dekra Certification).
Since 2010 he is consultant at Medical Device Project (MDProject – www.mdproject.nl), helping medical device manufacturers in Europe, USA, China and Israel on both quality and regulatory issues.
In addition to being a consultant, Mr. van Boxtel serves as a SME by the Dutch Norm Institute NEN, providing training on the MDD / MDR and ISO 13485.
Mr. van Boxtel has knowledge on non-active medical devices (cardiovascular, ophthalmology, orthopedics and more), and has experience with drug/device combination and animal tissue containing medical devices.

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