A single point of access for all your supporting Regulatory, Quality and Clinical Services
Our Regulatory Services will guide you through the various (inter)national and local regulations to assure compliance and access for the particular market of interest.
A sound quality management system in compliance with the (inter)national requirements will provide your company a structured method for your processes and aid in obtaining your certifications.
Our clinical strategy and trial support will provide you with a clinical strategy in line with the current expectations of the authorities to maintain state of the art clinical data.
Founded early 2015 by Robin J.M. Lucchesi and René Roncken,
MedQ Consultants B.V. main vision is to provide the medical device
Industry an option to have a single point of access for support in the
pathway from R&D to market access and beyond for their medical device
in a tailor-made project.
MedQ Consultants B.V. provides a broad range of regulatory, quality, clinical and Authorized Representative services for the medical device industry in order to provide an economic and practical approach in supporting your business through the duration of the project and life-cycle of your device.