Adult Cystic Fibrosis Conference

1-2 December 2023 | Milan, Italy | #ACFMilan2023

The conference will feature scientific sessions and interactive educational content, with a programme which has been developed to promote the diagnosis, treatment and ongoing management of cystic fibrosis.



Conference format

On-site participants benefit from: 

  • Cutting-edge scientific sessions 
  • Interactive educational content 
  • Access to international experts 
  • Networking opportunities 
  • Possibility to submit cases and abstracts for presentation and discussion


Topics covered include: 

  • Adult cystic fibrosis 
  • Monitoring and treatment from infancy to adulthood 
  • Management (quality of life) 
  • Gastrointestinal disease 
  • Diabetes 
  • Pregnancy and fatherhood 
  • Transplantation  
  • New therapies, latest research 


Live streaming and replays

Live streaming and replays will be available to both on-site and online participants. Please note that replays of live streamed sessions will be available after the event, in case you are unable to watch the sessions live.


The following sessions will not be live streamed:

  • Meet the Experts
  • Oral presentations
  • Case-based sessions


Faculty guidelines

Session typeInstructionsTemplate
Pro and Con debate
Meet the expert

Faculty guidelines

PowerPoint template
Case-based session
Faculty guidelinesPowerPoint template
Oral presentationFaculty guidelines-



Live event:

This event has been granted 11.5 CME credits for onsite attendance by the European Board for Accreditation in Pneumology (EBAP).


The number of credits that you will receive corresponds to your attendance during the conference. Please note that you need to sign the register of attendance each day to ensure that you receive the CME credits.


Online attendance:

Participants of the live stream can claim up to 10.5 CME credits for the hours spent viewing the sessions live.


Participants will not accrue credits for watching session replays.



In partnership with the European Cystic Fibrosis Society

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