Selection of Centres/Clinicians
Each participating centre (and Investigator) has been identified on the basis of:

  • Being a paediatric cystic fibrosis (CF) treatment centre
  • Having at least one lead clinician with a specific interest in, and responsibility for supervision and management of paediatric patients with CF
  • Showing enthusiasm to participate in the study
  • Ensuring that sufficient time, staff and adequate facilities are available for the trial
  • Planning to provide information to all supporting staff members involved with the trial or with other elements of patient management
  • Confirmation that they have a number of eligible patients
  • Acknowledging and agreeing to conform to the administrative and ethical requirements and responsibility of the study including adhering to GCP and other regulatory documentation


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