Jorrit Boersen

Jorrit Boersen is a Regulatory Affairs Specialist at NICO.LAB. Jorrit has over 6 years of experience in the medical device and IVD industry. Jorrit’s experience includes working as a Clinical & Regulatory Consultant, Medical Writer II, and Medical Writer I. In these roles, Jorrit was responsible for preparing and reviewing technical documentation for regulatory submissions in Europe, designing pre- and post-market clinical studies, creating training presentations on post-market clinical follow-up requirements of medical devices in the EU, performing gap analysis between EU Medical Device Directive and EU Medical Device Regulation, and training other medical writers.

Prior to working in the medical device industry, Jorrit completed a PhD in Technical Medicine at St. Antonius Hospital Nieuwegein in The Netherlands. Jorrit also holds a Master’s degree in Technical Medicine from St. Antonius Hospital Nieuwegein.

Jorrit Boersen holds a Master of Science in Technical Medicine from Universiteit Twente / Twente University. Prior to that, they studied at Christelijk Lyceum Veenendaal.