AbroadLink Translations Sponsors the TEAM-PRRC 4th Annual Summit 2025 in Rome

After our rewarding experience last year in Málaga, AbroadLink Translations is excited to announce our sponsorship and participation at the TEAM-PRRC 4th Annual Summit 2025, taking place in Rome, Italy, on October 23–24, 2025.

This leading European regulatory affairs event has become a cornerstone for professionals working with medical devices, in vitro diagnostics, and MDR/IVDR compliance. It is where top experts gather to share knowledge, discuss challenges, and shape the future of regulatory frameworks in the Life Sciences industry.

Who is TEAM-PRRC?

TEAM-PRRC (European Association of Person Responsible for Regulatory Compliance) is the main European association representing the Person Responsible for Regulatory Compliance (PRRC) role.

Introduced under the EU Medical Device Regulation (MDR 2017/745) and the In Vitro Diagnostic Regulation (IVDR 2017/746), the PRRC ensures that manufacturers meet strict regulatory and quality requirements before placing products on the European market.

The mission of TEAM-PRRC is to:

• Support PRRCs across Europe with training, resources, and regulatory guidance.
• Promote compliance best practices in medical device and diagnostic companies.
• Strengthen patient safety through effective oversight and accountability.
• Create a network of experts for knowledge-sharing and collaboration.

Today, TEAM-PRRC has become the go-to community for regulatory compliance professionals in the EU medical device industry.

Why the TEAM-PRRC Summit 2025 in Rome is a Must-Attend Event

The TEAM-PRRC Annual Summit is recognized as one of the most important regulatory affairs conferences in Europe. Here’s why it stands out:

• Latest EU MDR/IVDR updates – Stay informed about new regulatory requirements and notified body expectations.
• European networking hub – Meet regulatory affairs experts, medical device manufacturers, consultants, and service providers.
• Practical insights – Interactive sessions provide hands-on solutions for navigating compliance challenges.
• Future-oriented topics – Discussions highlight how regulatory frameworks can foster innovation and safer healthcare solutions.

If you are involved in medical device compliance in Europe, this summit is a key opportunity to strengthen expertise and partnerships.

About AbroadLink Translations – Specialists in Life Sciences and Medical Devices

At AbroadLink Translations, we support Life Sciences companies with specialized translation services for medical devices, clinical trials, and regulatory documentation.

We are proud to hold three ISO certifications that guarantee quality and compliance:

• ISO 9001 – Quality Management Systems
• ISO 17100 – Translation Services
• ISO 13485 – Medical Devices Quality Management

With this expertise, we help:

• Medical device manufacturers comply with EU MDR/IVDR requirements across multilingual markets.
• Life Sciences companies expand globally with precise, industry-specific translations.
• Regulatory teams avoid risks through accurate, certified documentation translations.

By combining linguistic excellence and regulatory know-how, AbroadLink is the trusted partner for companies navigating compliance in Europe and beyond.

TEAM-PRRC 4th Annual Summit 2025 – Event Details

Location: Rome, Italy
Dates: October 23–24, 2025
Focus: EU MDR/IVDR compliance, medical device regulation, PRRC role

As a sponsor and exhibitor, AbroadLink Translations will be on site to connect with regulatory professionals, manufacturers, and innovators in the Life Sciences industry.

Following our successful participation at RAPS Euro Convergence 2025 in Brussels, we are eager to continue engaging in meaningful conversations, tackling regulatory challenges, and showcasing how our specialized regulatory translation solutions can support MDR/IVDR compliance and international growth.

Are you attending the TEAM-PRRC 4th Annual Summit in Rome? Visit us at our stand and let’s discuss how expert medical device translations can help your organization stay compliant, expand globally, and build safer healthcare systems.