Class definition for your medtech product.
Establish a quality management system.
Risk management plan for CE Marking and/or FDA clearance.
Clinical evaluation to prepare your trial designs, show you the optimal time to apply for approval, and more.
Build your strategic roadmap for evidence demonstration and registration dossier filing.
Access to market coaching, to identify target populations and estimate potential pricing.
Understanding CE mark vs. FDA requirements, because Neighborhood and VCLS are built with one foot firmly planted on each side of the Atlantic, we can show you all the intricacies of both processes.
Digital Option
Digital Medical Device conception (62304 implementation)
Establishing software under the Medical Device status is a challenge. Different standards apply, and “agile” development is possible under certain conditions. Let Neighborhood show you how.
IVD (In Vitro Diagnostic) Option
Implementation IVDR 2017/746/EU
The development of an IVD follows a specific regulation which is constantly evolving. Neighborhood can help you meet these requirements.
Dedicated Team
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