Expertise
Additude Medtech Solutions
Northern Europe´s nr. 1. go-to provider in Medtech development services
The Team
Our MedTech team consists of a unique combination of expertise in engineering, management and medical compliance knowledge. Collectively, we have more than 100 years of experience within the MedTech domain and a vast experience of the added complexity of complying with the Medical Device Regulation (MDR).
Offerings
We can take your business idea from user need/concept to market, using our experience of all aspects in development and manufacturing of Medical Devices.
- In-House Product Development
- Project Management
- Interim Management
- Clinical - Technical Translation
- Secondment
- Design Transfer and Production Establishment
- Technical Due Diligence
Certifications
We have several years of experience working according to:
- MDR (Medical Device Regulation)
- ISO 13485
- QSR
- ISO 14971
- IEC 60601
- IEC 62366
- IEC 62304
- And several collateral standards
All Additude's Business Areas
ICT Group Healthcare
As a part of ICT Group, Additude Medtech Solutions has access to an additional 1900 of Europe’s leading resources, in addition to the 200 from other Additude areas, from a variety of technical domains working together for a smarter world and sustainable future.