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Business case TI Pharma Mondriaan project

The TopInstituut Pharma wanted to know if there would be a professional justification for the Mondriaan project following the completion of the project phase in 2012.

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The question

Industrial and academic research teams work together on the project Mondriaan in order to develop an infrastructure for coupling existing pharmaceutical, medical/clinical and care data in the Netherlands. The aim is to make data available for scientific research in the field of effectiveness and safety of medicines.

What InnoTact did

InnoTact identified the potential interested parties for the future infrastructure. We presented the achieved and intended project results in order to explore their interest in the formation of the infrastructure.

The conclusion was that the Mondriaan initiative could create a position for itself within the landscape of health research in the Netherlands. The aim was to achieve clear-cut demarcation and transparent products, in combination with defining markets. We developed these and evaluated them against the ideas of the project team.
We asked the ‘outside world’ about the added value of this type of design for Mondriaan. We also gained an insight into the potential forms of compensation to data suppliers, the scope of the market and the value of the datasets during this round of interviews.

We made recommendations in respect of the strategy and positioning for Mondriaan that will lead to a financially independent entity that can successfully participate in the business sector traffic after 2011. And the setup of the organisation and operations to support this.

The result

During the remaining 2.5 to 3 years of the project, the responsible persons know which choices have to made and which action must be undertaken in order to facilitate the structural continuation of the Mondriaan initiative after 2012. This infrastructure for coupling the existing pharmaceutical, medical/clinical and care data is a strong contributory factor to the TI Pharma objective: to shorten the expensive ‘drug’ development process and simultaneously reduce the risks of ‘clinical failure’ of new medicines.

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