ENETS NET Registry Aims and Mission

The Registry is part of the European Neuroendocrine Tumor Society (ENETS) and was established in 2007. The Registry is managed by the Working Group. The members of the Registry Working Group are appointed by the ENETS Executive Board and they have to be members of ENETS.

The Working Group consists of representatives from different European nations. 

The Registry Mission

To support ENETS in the creation, development, maintenance and expansion of a large multinational common database on NET. 

The aims are to:

  • collect data on patients with NET in a secure and complete way
  • provide an efficient and scientific valid data analysis
  • guarantee data integrity and patient privacy
  • approach unanswered questions on the management of NET by performing hypothesis driven data analysis
  • create a network of participating physicians



Important Notice:

In preparation of the upcoming 16th Annual ENETS Conference, 6 to 8 March 2019 in Barcelona, Spain, we have discovered in the world wide web at least one professional entity suggestive of possessing an ENETS mandate for conference registrations. Therefore, we must inform you that 100% of all conference participants are registered through ENETS official website www.enets.org and http://enetsconference.org/. There are no further options to validly register for Barcelona 2019 (or for any other ENETS event).

Please stay away from fraudulent scams abusing the ENETS acronym to register – and charge you above official ENETS conference fees! Such entities, against whom ENETS presses criminal charges, are neither authorized, nor commissioned nor instructed by ENETS to make such representations.