The authorization referred to in Article (17) of this Decree by Law may only be granted to the following entities: 1. Government authorities and recognized institutes. 2. Licensed health establishments. 3. Licensed chemical analysis laboratories or medical, scientific, or industrial research laboratories. 4. Warehouses and storage facilities of medical products, public pharmacies, compounding pharmacies, medical products manufacturing facilities and contract manufacturing organizations, contract research and development organizations, and licensed non-clinical and clinical research entities, provided that they have a licensed responsible pharmacist authorized to practice the profession. 5. Offices of brokers and agents of medical product factories and companies licensed to engage in such activity, provided that they have a licensed responsible pharmacist authorized to practice the profession. The authorization shall be issued in the name of the director of the entity or the person responsible for it in their official capacity, based on a signed application submitted using the form prepared by the Competent Administrative Authority for this purpose. The said Authority may refuse to grant authorization or reduce the requested quantity.
Interpretation and application must be checked against the official text and current version.