European MedTech Regulatory
MedTech Europe
MedTech Europe is the European trade association for the medical technology industry, advocating for policies that support innovation and patient access to advanced healthcare solutions.
MedTech Europe serves as the primary European trade association for the medical technology industry, encompassing diagnostics, medical devices, and digital health. Its core mission is to facilitate the availability of innovative medical technologies to a broader population while assisting healthcare systems in transitioning towards sustainability. The association actively promotes policies that enable the medical technology industry to meet Europe's evolving healthcare demands and expectations. Through economic research, data analysis, communication strategies, industry events, and training, MedTech Europe champions the value of medical technology, with a particular emphasis on innovation and stakeholder relations. Originally formed in October 2012 as an alliance of EDMA (European In vitro diagnostic industry) and Eucomed (European medical devices industry), MedTech Europe has grown to represent a significant sector crucial for modern healthcare. The organization actively engages with healthcare stakeholders on critical issues such as regulations, market access, digital health, and Brexit. It also focuses on addressing challenges related to sustainable healthcare systems and fostering dialogue about medical technologies. MedTech Europe plays a vital role in shaping the future of healthcare by advocating for a more efficient, proportionate, and predictable regulatory system for medical technologies across Europe.
About
**Who they are**
European MedTech Regulatory is the European trade association for the medical technology industry. They advocate for policies that support innovation and patient access to advanced healthcare solutions.
**Expertise & scope**
* Representing the medical technology industry across Europe.
* Focusing on policies that foster innovation.
* Working to ensure patient access to advanced healthcare solutions.
**Reputation / proof points**
* Coverage across the EU.
* Services available in English, French, Dutch, German, Italian, and Spanish.
European MedTech Regulatory is the European trade association for the medical technology industry. They advocate for policies that support innovation and patient access to advanced healthcare solutions.
**Expertise & scope**
* Representing the medical technology industry across Europe.
* Focusing on policies that foster innovation.
* Working to ensure patient access to advanced healthcare solutions.
**Reputation / proof points**
* Coverage across the EU.
* Services available in English, French, Dutch, German, Italian, and Spanish.
Additional information
European MedTech Regulatory focuses on shaping the policy landscape for medical technology in Europe. Their work involves advocating for regulatory frameworks that balance innovation with patient safety and access. Buyers engaging with this association can expect a focus on industry-wide policy and advocacy rather than direct service provision for individual product compliance.
HQ:
Brussels, Belgium
Website:
eumetechregulatory.com
Public email:
info@eumetechregulatory.com
Phone:
0508570208
Languages:
English, French, Dutch, German, Italian, Spanish
Timezones:
CET, CEST
Status:
pro
Services & Capabilities
PRRC MDR (EU MDR) | PRRC Medical Device Service | Compare Providers & Get Quotes
Jurisdictions:
EU
Countries:
BE, FR, DE, IT, ES, NL, PL, CZ, AT, SE
Industries:
Medical Devices, IVD, SaMD, Combination Products
Response SLA:
24 hours
Onboarding time:
7–14 days
Pricing model:
per_market
Starting from:
EUR 2,000
Included services:
Named PRRC, Multi-country support, Technical documentation review, Regulatory strategy
Named PRRC:
No
