Leading the Way in Product Development & Design
With strong competencies in R&D combined with regulatory, quality and project management, Mgs Design & Development is comprised of an innovative and skilled team of experts who share a passion for developing high-quality products in the Pharma and MedTech industries.
Each team member shares a pioneering spirit, driven by the desire to improve and change the lives of patients around the world. Leveraging its deep industry expertise, every team member collaborates with partners, clients and employees to accelerate long-term success.
Centrally located in Denmark, this location houses expertise across project scoping, project management, mechanical engineering, simulation and modeling, test and verification, user experience and design, sustainability and usability engineering, design control, and more.
MGS Design & Development, formerly Technolution, started with a simple wish to improve the industry and make Pharma & MedTech even better. It happened with a pioneering spirit, which is still alive and influencing our constant drive for developing products, designed to improve lives of people around the world.
As specialized nerds, we believe that agility should be at the heart of what we do. Our core is product development, which demands innovation and teamwork. No solo effort could have brought us to where we are today. That’s why our specialized design and development teams are organized under a strategic umbrella fostering co-leadership, leveraging individual strengths and nurturing collaboration across areas of expertise that we call Circles.
MGS Design & Development delivers critical upfront product design and development expertise from a prominent Medical and Life Sciences hub in Europe. Our team integrates seamlessly with experts in tooling, automation and manufacturing to deliver true end-to-end solutions for Pharma, Diagnostics and MedTech innovators.
Exceeding Healthcare Manufacturing Quality Standards
Technolution is in compliance with ISO 13485, risk management procedures according to ISO 14971, and Usability Engineering activities according to IEC 62366-1. Furthermore, the team works with a wide range of device-specific standards to ensure your Pharma, MedTech and Diagnostics devices fulfill all critical requirements and regulations.
