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

 

 

Close
Notice

Dear conference participant,

Thank you for participating in the ENETS Virtual Conference 2020!

You now have the opportunity to view the webcasts, abstracts and e-posters via My ENETS. Don't miss out any of the exciting talks and take your time to view the clinical and basic science abstract sessions.

If you require a certificate of attendance, please log into My ENETS and select “Annual Conferences” from the side menu, then click on “My registrations” and select your registration for 2020. Please choose "Certificate o.A." to receive your certificate of attendance.

A note on CME accreditation:

ENETS has been liaising with UEMS regarding CME accreditation for the virtual conference. At present, we do not have a definitive answer. We will keep you updated.

 

Wishing you all the best,

The entire ENETS team