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PMV-EU provides comprehensive services for medical device manufacturers, focusing on regulatory compliance, quality management, and market access in the European Union and beyond. They offer solutions tailored to help clients navigate the complex landscape of medical device regulations, ensuring product safety and efficacy.
Serves as the central hub for management, research, development, and administrative functions.
Modern office space designed to foster collaboration and innovation.
The headquarters fosters a collaborative and innovative work environment, emphasizing teamwork, continuous learning, and a commitment to quality and compliance. Employees are encouraged to contribute to the company's mission of improving patient outcomes through safe and effective medical devices.
Berlin was chosen as the location for its strong medical technology ecosystem, access to talent, and strategic location within the European Union.
PMV-EU supports clients globally with regulatory compliance services, focusing particularly on the European Union, United States, Switzerland and other key markets. They offer expertise in areas such as regulatory strategy, CE marking, FDA submissions, and quality management systems.
Tempelhofer Weg 11-12
Berlin
Berlin
Germany
Address: Talstrasse 64, 8955 Hüttikon
Serves as a hub for regulatory affairs and customer support for the Swiss market.
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As of April 2025, PMV' leadership includes:
PMV has been backed by several prominent investors over the years, including:
Limited information available on recent executive hires/exits within the last 12 months. Requires further investigation.
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PMV-EU's email format commonly follows a pattern using the first initial and last name. Note that this can vary based on the person.
[first_initial][last]@pmv-eu.com
Format
vbutz@pmv-eu.com
Example
90%
Success rate
LinkedIn • 2023-05-10
PMV-EU shared an update regarding the new Medical Device Regulation (MDR) guidelines, highlighting key changes and implications for manufacturers....more
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