Develop MDR-compliant medical devices to improve the lives of many people
Work with experienced movers and shakers from medical technology, regulatory affairs and management.
For MedTech Companies
What challenges do you face in the development of medical devices?
Are you overwhelmed by the vulnerabilities that are being revealed in your organization as part of the MDR transition?
Is your team frustrated by the many regulatory requirements and doesn’t know how to implement them?
Are the required competencies – from product development to approval & QM – available and sufficiently available in your company?
Are you struggling with significant unplanned delays and cost increases on your development projects?
In view of the complexity and multiplied efforts, are you afraid that you will no longer be able to develop innovations in the future?
Do you feel that your company’s growth is too operational and not strategic?
At 3R LifeScience, we ensure that you have full control over the development of your products and your company despite of the coming MDR.
How to use the transition to the MDR as an opportunity for sustainable optimization of your processes and portfolio.
R&D + MedTech Product Development
How to realize innovations in medical technology efficiently and in compliance with legal requirements, and how to make product development fun again.
Quality management & Regulatory
How to achieve your regulatory goals holistically and economically and make quality management a profit guarantor.
Business Developement & Financing
How to gain clarity on your business goal and lead your business to success without detours.
Realize your project in 3 easy steps
It is best to make an appointment today for a free initial consultation.
One of our experts will clarify your requirements and questions with you in the appointment.
If cooperation is possible, we will arrange a workshop with you.