Hartwig Medical Foundation

To make the right treatment decision, cancer specialists need to collect all the available diagnostic information from the patient and their tumor.

We are contributing to this work by:

Developing

innovative molecular tests, for identifying the characteristics of the tumor.

Collecting and storing

knowledge of and information about the patient and their tumor.

Integrating

the information and knowledge with treatment outcome to accelerate scientific research. This enables us to learn from the data of today’s patients and provide better treatment for the patients of tomorrow.

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Your contribution to improving the treatment of tomorrow’s patients is important. Share your data, too!

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United in Unique – every individual story is unique

United in Unique – every individual story is unique

05-02-2026

On World Cancer Day, attention is drawn worldwide to the impact of this disease This year’s theme, United in Unique, highlights the fact …

Care pathway broad molecular diagnostics approved, important step forward

Care pathway broad molecular diagnostics approved, important step forward

05-02-2026

On World Cancer Day, we reflected on the enormous impact of cancer. But this impact is visible every day—on patients, their …

The role of molecular diagnostics in sarcomas 

The role of molecular diagnostics in sarcomas 

05-02-2026

Between Science and Clinical Practice  The use of molecular diagnostics in sarcoma care is receiving growing international attention. Recent studies¹ …

Comprehensive molecular diagnostics closer for more patients thanks to price reduction 

Comprehensive molecular diagnostics closer for more patients thanks to price reduction 

20-01-2026

Hartwig Medical Foundation reduces the price of its OncoAct Whole Genome Sequencing (WGS) service as of January 1, 2026. This …

New research shows a more significant role of genetic predisposition in adults with glioblastoma

New research shows a more significant role of genetic predisposition in adults with glioblastoma

16-12-2025

A recent study published in npj Genomic Medicine shows that hereditary predisposition in adult glioblastoma patients is more common than …

Large-Scale UK study confirms clinical value of Whole Genome Sequencing in breast cancer

Large-Scale UK study confirms clinical value of Whole Genome Sequencing in breast cancer

15-12-2025

A recent publication in The Lancet Oncology (October 7, 2025) shows that Whole Genome Sequencing (WGS) is ready for large-scale …

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Listening, connecting, and building bridges to make more impact for patients with cancer

Listening, connecting, and building bridges to make more impact for patients with cancer

19-01-2026

This is how Robert Jan Lamers describes his role as managing director of Hartwig Medical Foundation. For four months now, …

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Medicines Policy must be based on real world data 

Medicines Policy must be based on real world data 

15-08-2025

The recent decision by the National Health Care Institute to re-evaluate expensive cancer medicines in real-world practice is a logical …

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Cancer, a rare disease?

Cancer, a rare disease?

28-02-2025

It may come as a surprise to many on this International Rare Disease Day (February 28), that a significant number …

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