Applicant establishments or organisations are required to have:
1° Premises fitted out, arranged and maintained in accordance with the rules of good practice provided for in the first or third paragraph of Article L. 5121-5 and, where applicable, in accordance with the containment requirements adopted in application of Article L. 532-1 of the Environmental Code;
2° Staff whose skills and qualifications comply with these rules of good practice;
3° Equipment complying with these rules of good practice to guarantee the quality, health safety and traceability of medicines and to reduce as far as possible any risk to patients and staff.