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Heart Failure Guidelines Forum October 13 & 14 2016 – 4th edition


Why a Heart Failure Guidelines Closed Forum?

The quality of research and development efforts made by manufacturers of pharmacological agents, biomarkers, and medical devices has obviously had a major impact on the position of these products in clinical guidelines on the management of heart failure. Conversely, the success and failure stories that inevitably accompany the release of new guidelines may be a source of inspiration for further research and development. And, ultimately, guidelines really shape clinical practice if doctors and their patients adopt them.

A better understanding of the processes involved in guidelines development will help companies that develop drugs, biomarkers, and devices to adapt and improve their research and development programmes for the future. This could also translate into earlier and more efficient development of diagnostic and therapeutic tools for patients.

Scientific Program

How do guideliners deal with the available evidence and what are their expectations in this respect? What criteria must a product or an intervention meet to be recommended by heart failure guidelines? What are the most frequent reasons for failure? Why may guidelines of geographically distinct origins but dealing with the same evidence occasionally reach different conclusions? What should be done to avoid that guidelines being lost in translation?

Speakers and discussants who will address these topics have been selected from among the top-level European experts in cardiology who participate in the regular update of guidelines. The faculty also comprises clinicians with a strong interest in translational and patient-centered medicine.

The Heart Failure Guidelines Close Forum will be strictly academic – meaning that attendees will not participate during the main sessions and discussions. However, they will be able to transmit written questions to the faculty.

Without any doubt, the Heart Failure Guidelines Close Forum is a rare opportunity.

Don’t miss it!

Download the full program

General information


  • 1 attendee – 9,500 €
  • 2 attendees – 15,500 €
  • 3 attendees – 19,500 €
  • 4 attendees – 22,500 €
  • 5 attendees – 24,500 €

Includes attendance to the two day meeting, coffee breaks and lunches.

Early bird registration

15% off for a 6 month early registration

10% off for a 3 month early registration

Case based discussion

Support of a specific case based discussion (two experts from the faculty) during plenary session: 15,000 €.

On demand programs

For any special deliverable, or event please contact us:

TMA Foundation:

Charles Schoen – Tel.: + 33 (0) 6 08 18 77 08 – E-mail : charles.schoen@tm-academy-nonprod.medege.stage.beyondtec.co
Anne-Sophie Squiban – Tel.: +33 (0) 74 52 37 09 – E-mail: annesophie.squiban@tm-academy-nonprod.medege.stage.beyondtec.co

October 13 2016


Start: 13 October 2016
End: 14 October 2016
Event Category:



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