The elements of the programme include in particular:
1° The name of the medicinal product, together with its international non-proprietary name;
2° Information essential for the appropriation of the technical procedures required by the treatment and for the proper use of the medicinal product;
3° A reminder of the patient’s rights with regard to the programme, including the prior information to be provided to the patient and the form for obtaining the patient’s written consent, which includes:
a) The name and contact details of the healthcare professionals employed by the operator;
b) A statement to the effect that the personal data collected as part of the programme will only be kept for the duration of the patient’s participation in the programme.