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.

Vrouw en man spreken in behandelkamer met vrouwelijke arts, zittend aan een overlegtafel

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

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Share your data and share our vision for the future of cancer diagnosis

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Whole genome sequencing: the future of molecular diagnostics in gynecological cancer? 

Whole genome sequencing: the future of molecular diagnostics in gynecological cancer? 

30-09-2025

To mark Gynecological Oncology Awareness Month, we spoke with oncologist Eelke Gort about the role of molecular diagnostics in these …

GLOW Study Ends – But WGS Remains Valuable for Glioblastoma Patients

GLOW Study Ends – But WGS Remains Valuable for Glioblastoma Patients

29-09-2025

As of October 1, 2025, the GLOW study will officially come to an end. Interim analysis has shown growing enthusiasm …

Hartwig Medical Foundation welcomes new managing director

Hartwig Medical Foundation welcomes new managing director

04-09-2025

Hartwig Medical Foundation is pleased to announce that Robert Jan Lamers has joined the organization as its new managing director, …

Dutch Healthcare Institute approves reimbursement of whole genome sequencing (WGS) for targeted cancer treatment 

Dutch Healthcare Institute approves reimbursement of whole genome sequencing (WGS) for targeted cancer treatment 

15-08-2025

The Dutch National Health Care Institute (Zorginstituut Nederland, ZiNL) has approved the reimbursement of whole genome sequencing (WGS) through the …

Without structured real world data, it remains guesswork who truly benefits  

Without structured real world data, it remains guesswork who truly benefits  

15-08-2025

The decision by the Dutch National Health Care Institute (Zorginstituut Nederland, ZiNL) to reassess the reimbursement of expensive medicines after …

Update on the GENAYA Project: DNA from 500 Young Cancer Patients Analyzed

Update on the GENAYA Project: DNA from 500 Young Cancer Patients Analyzed

29-07-2025

Should young people with cancer receive different treatment than older patients? We suspect they do, but there’s currently not enough …

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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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The big advantage of having Hartwig Medical Foundation data available in the cloud

The big advantage of having Hartwig Medical Foundation data available in the cloud

10-03-2022

I don’t remember exactly when I first heard about Hartwig Medical Foundation and the whole genome sequencing data it has …

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