The holder of the authorisation has the following facilities on the site:
1° At least one hospitalisation sector;
2° At least one technical platform for administering intravenous treatments;
3° Medical and paramedical consultation rooms;
4° An in-house pharmacy authorised to prepare anti-cancer drugs within a centralised cytotoxic preparation unit that complies with the recommendations for good practice issued by the Agence Nationale de Sécurité du Médicament et des Produits de Santé. If the holder does not have an in-house pharmacy or a centralised cytotoxic preparation unit, the preparation is carried out under a subcontracting agreement with another establishment authorised to prepare anti-cancer drugs within a centralised cytotoxic preparation unit.
For holders of a B or C authorisation, the hospitalisation sector provided for in 1° must include individual rooms equipped with air decontamination devices for malignant haemopathies or malignant solid tumours whose treatment by intensive chemotherapy results in foreseeable aplasia lasting more than eight days.