Qserve has considerable in-house regulatory affairs expertise in the areas of medical device regulatory affairs.

Medical Devices

Qserve

Jan van Lochem

Patrick Bouwman

Martin de Bruin

Pim Kolsteeg

Mindy McCann

Keith Morel

This department oversees compliance and quality assurance related to medical devices, ensuring adherence to regulations.

Regulatory Affairs

This department provides expert advisory and consulting solutions to clients, leveraging various levels of experience and expertise.

Consulting Services

This department oversees the planning, execution, and management of clinical trials to ensure they meet regulatory standards and organizational goals.

Clinical Operations

This department manages and oversees the registration processes and legal compliance on a global scale.

Global Registrations

The Marketing and Business Development team at Qserve is dedicated to expanding the company's market presence and driving growth within the medical device regulatory affairs sector. They work collaboratively to develop strategic marketing initiatives, manage communication channels, and foster partnerships in key regions, leveraging their expertise to connect with clients and stakeholders effectively. This team plays a crucial role in promoting Qserve's services and contributing to its overall business strategy.

Marketing and Business Development

This department focuses on analyzing data and managing application systems to drive informed decision-making and improve operational efficiency.

Qserve

Org chart

Teams

Regulatory Affairs

Consulting Services

Clinical Operations

Global Registrations

Marketing and Business Development

Analytics and Applications

Offices

Qserve

Org chart

Teams

Regulatory Affairs

Consulting Services

Clinical Operations

Global Registrations

Marketing and Business Development

Analytics and Applications

Offices

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