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International project management for medical devices

Discover how our international project management for medical devices combines global expertise with local insight to support efficient processes, regulatory compliance, and successful project outcomes.

Contact our project management today
TÜV NORD´s Project management circle

What makes our international project management for medical devices unique?

The international project management for medical devices is a global network of experienced project managers supporting organizations in the healthcare and medical device sector. Our team has extensive expertise in a wide range of services, including medical devices (MDR 2017/745), in vitro diagnostics (IVDR 2017/746), and quality management systems such as ISO 13485, EN 15224, and ISO 7101, as well as healthcare-related services like reprocessing of medical devices and Good Distribution Practice (GDP).

Our project managers act as central points of contact, ensuring that every project is efficiently coordinated, and successfully executed. Leveraging our global presence, the project management combines international oversight with local expertise, simplifying the management of regional requirements and cultural differences.

They support your success anywhere in the world and at every stage of your project with a strong focus on partnership, transparency, and efficiency.

What are the tasks of our global project management?

Our international project management supports the entire certification journey, including:

  • Development and optimization of certification programs
  • Audit preparation, execution, and follow-up
  • Implementation of the four-eyes principle and approval processes
  • Certificate initiation and lifecycle management
  • Resource planning and allocation
  • Risk identification and mitigation

Contact

Are you interested in our services or have questions about our international project management for medical devices?
Linda Harvey, TUV USA

Linda Harvey

Project Management Team Lead at TUV USA, Inc.

TUV USA MDR & IVDR Booklets

MDR Booklet


This booklet offers a full overview of the EU Medical Device Regulation (MDR) and includes the latest M5 amendment.

IVDR Booklet


This booklet offers a full overview of the In Vitro Diagnostic Regulation (IVDR), including the latest amendments and updates.