ENETS NET Registry

ENETS has set up a European multi-national registry for patients with neuroendocrine tumours (NET) under the name of ENETS European NET Registry to enhance and foster multicentre, multinational investigations to collect and deliver information on the efficacy and safety of diagnostic and therapeutic strategies to care for or treat NET and to scientifically investigate the epidemiology of NET.

The Registry uses observational study methods to collect uniform data (clinical and other) to evaluate specified outcomes that serves one or more predetermined scientific, clinical, or policy purposes.

In addition, the Registry documents and analyses the quality of care, the differences in care related to various European Health Care Systems, and the effect of different therapeutic strategies on the long term outcome of NET.

The Registry aims at improving the documentation of the disease, developing a quality-management system for the diagnosis and therapy of NET.

In case your country has already a national NET database, a transfer of the data into the ENETS registry is possible.

In case your country does not have a registry, the ENETS registry offers the possibility to perform direct inclusion of patient data.

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WARNING – FRAUDULENT WEBSITES

ENETS is aware that its members have been confronted with fake websites, which seem to relate to our congress but have not been commissioned or authorised by us. The websites offer fraudulent hotel reservation services. We therefore strongly recommend that you please only use the official enetsconference.org website when booking your tickets and accommodation. Please be vigilant when it comes to providing your credit card details. 

If you have any questions, please do not hesitate to contact us at info@enets.org.