Interdos is part of the Basic Pharma Group located at the Brightlands Chemelot Campus in Geleen, the Netherlands.

Interdos is your trusted partner for Regulatory Affairs (RA), Pharmacovigilance (PV), Quality Assurance (QA), and Laboratory services in the global pharmaceutical industry. With over two decades of expertise, we deliver proven solutions worldwide.

The team of Interdos is your perfect partner in guiding you through national or international procedures/legislations regarding pharmaceutical RA, QA, PV and laboratory testing. We have the know-how, the equipment, the experience and the network to direct you from development process towards approval and beyond.

For additional information or to get in touch, please visit our website. We are more than willing to assist you.

Health Care

Life Sciences

Pharmaceutical

Interdos

Interdos' headquarters in Geleen, Netherlands

Berend Ros

Wendy Verschuren - Creemers

Heleen Kessels

Daniëlle Willems

The Regulatory and Pharmacovigilance team at Interdos ensures that pharmaceutical products comply with national and international regulatory requirements and safety standards. They manage the entire lifecycle of regulatory submissions, monitor drug safety through pharmacovigilance activities, and ensure ongoing compliance post-approval. This team leverages its extensive expertise to navigate complex procedures, mitigate risks, and uphold high-quality standards in the global pharmaceutical industry.

Regulatory and Pharmacovigilance

This department manages compliance with regulations and oversees the approval processes for products.

Regulatory Affairs

This department ensures that products meet quality standards and regulatory requirements through rigorous testing and oversight.

Interdos

Org chart

Teams

Regulatory and Pharmacovigilance

Regulatory Affairs

Quality Assurance

Offices

Interdos

Org chart

Teams

Regulatory and Pharmacovigilance

Regulatory Affairs

Quality Assurance

Offices

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