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Vincent Rothuizen has a diverse range of work experience. Vincent most recently worked as a Data Analyst at Avania, a contract research organization specializing in managing clinical studies for medical devices and biologics. Prior to that, they completed a graduation project at Sentron Europe B.V., a Wellinq company. Vincent also has experience working in retail as a Sales Assistant and completed an internship at UMCG Centrum voor Revalidatie. Vincent gained further experience through various projects and roles as a student assistant and volunteer at the University of Groningen. Additionally, Vincent worked as a Representative for Knaek Promotions and volunteered at Rode Kruis District Groningen.

Vincent Rothuizen's education history is as follows:

Vincent Rothuizen attended the University of Groningen from 2009 to 2011, where they obtained a propedeuse in Pharmacy. Vincent then pursued a Bachelor's degree in Human Movement Sciences from 2012 to 2016 at the same university. Vincent continued their education at the University of Groningen, earning a Premaster degree in Biomedical/Medical Engineering from 2016 to 2017. Vincent further pursued a Master's degree in Biomedical Engineering from 2017 to 2019, completing their education at the University of Groningen.

In addition to their academic degrees, Vincent Rothuizen has obtained several certifications. In 2011, they acquired the certification for Safe Microbiological Techniques (VMT) from the University of Groningen. Vincent also completed a course on Patientveiligheid en technologie/Patient safety and technology in 2018, which was offered jointly by the University of Twente and the University of Groningen.

Furthermore, Vincent has obtained multiple certifications from the World Medical Device Organization (WMDO) in 2020. These include certifications in The European Union Regulatory System for Medical Devices, ISO 13485:2016 - Medical Devices Quality Management Systems Requirements for Regulatory Purposes, Designing a Strategic Medical Device Clinical Investigation Plan/Protocol, Overview of Data Management Plan and Query Process, Adverse Event Processes, Clinical Evaluation of Medical Devices: an Introduction, Clinical Events Committee (CEC) Establishment, Data Safety & Monitoring Board (DSMB) Establishment, European Safety Reporting Requirements during Pre-Market clinical Investigations, Introduction to Good Clinical Practice, Medical Device GCP: A Practical Summary, Source Document Verification, Steps to CE Mark, and ISO 14155:2020 – A Summary Review.