About QMedCo
QMedCo offers Clinical Evaluation consulting, primarily for SMEs, start-ups, and early-stage medical device firms. We provide strategic guidance on all aspects of their Clinical Development Plan. All activities are aimed to achieve time & cost efficient clinical trials to deliver robust clinical data to fully comply with the European MDR regulations for successful CE mark attainment.
Personal and dedicated approach
QMedCo is a boutique consultancy mainly focusing on the challenges SME's, start-ups and early stage medical device companies face with implementation of the MDR regulations. We offer highly personalised and dedicated project management. Unlike larger CRO's, QMedCo works with a selected number of clients a year, in close partnership, where our senior consultants will ensure your project is delivered in a cost and time efficient manner for your business.
Let me introduce myself
Michel de Wildt MD | PhD | MBA
Founder and Principal Consultant
Michel is the director & founder of QMedCo, a boutique consultancy company with the mission ‘to support its clients efficiently and effectively by delivering the most impactful and relevant clinical data for their business operation’.
He has a strong track record in Clinical Evaluation of medical devices where for more than 10 years he was the medical director of a clinical trial company.
As a practising consultant urologist, he personally knows the practical aspects of clinical devices with decades of clinical experience in both academic and tertiary referral centers.
He is an author in 60 peer reviewed papers, mainly on clinical research of medical devices.
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