Customer Focus and
Flexible Collaboration
At MedRes, we employ a rigorous development process to ensure that our devices meet the highest standards for safety and efficacy.
Our contract development services are tailored to the specific requirements of each project, and include ideation, design and concept development, prototyping, testing, engineering support for regulatory and clinical development processes, transfer to pilot production and volume manufacturing.
1. Ideation & Design
2. Product Development
3. Clinical & Regulatory compliance
4. Pilot Production & Manufacturing Ramp Up
Contract development services
Ideation & Design
First, your product idea is explored in the context of specific clinical and market needs. Target use cases and markets are researched, and product concepts are developed through continuous idea generation, testing, and refinement cycles until a feasible solution is reached — all in close cooperation with you.
Product Development
User and patient needs are analyzed to design ergonomic, intuitive interfaces. Product development is completed with Design for Manufacturing principles in mind, while supply chain requirements are carefully considered in material selection and packaging design.
Clinical & Regulatory compliance
Pilot units are built and pre-clinical and clinical testing is supported to meet regulatory requirements, with documentation compiled for EU or US submissions.
Pilot Production and Manufacturing Ramp Up
A fully documented, volume-capable manufacturing line is established. Product-specific tools and equipment are developed and built, and your product is seamlessly integrated into the supply chain solution.
Areas of Expertise Within Our Team
Our team’s diverse composition allows for a comprehensive approach right from the idea’s inception, considering function, safety, ergonomics and integration with other tools and instruments right form the very beginning.
Housing product designers, mechanical, software and electrical engineers, and specialists in hardware and firmware, our multifaceted teams ensure that every detail of medical device development is covered by a colocated team, eliminating delays and reducing loss of information in team communication.
Inhouse biological researchers, biomedical engineers on our teams bridge complex engineering concepts with real-world medical needs, ensuring that products are precisely tailored to actual clinical needs and use scenarios.
Our focus on quality is uncompromised. V&V and Documentation Engineers meticulously manage technical documentation, while our hands-on technicians guarantee precision throughout the compilation of Technical documentation files and design history files.
Our Grants

Grant ID: 2018-1.1.2-KFI-2018-0014
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