Authorisation may only be granted if the holder has:
1° An on-site interventional sector;
2° On-site access, by agreement or, where applicable, as part of the shared medical project of the regional hospital grouping referred to in II of Article L. 6132-1, access to the following services within a timeframe compatible with the safety of treatment:
a) Medical biology examinations;
b) Anatomopathology examinations;
c) Medical imaging examinations;
d) Labile blood products.
3° On site, by agreement, where applicable as part of the shared medical project of the regional hospital grouping mentioned in II of Article L. 6132-1, access to a critical care unit or, where applicable, a formalised internal procedure for transferring patients to a critical care unit, enabling them to be cared for within timescales compatible with the imperatives of care safety.
4° An organisation enabling the application of articles R. 6111-18 to R. 6111-21 and ensuring the availability of sterile medical devices, particularly in emergency situations.