[en] Once installed and accepted, a system for stereotactic radiosurgery / stereotactic radiotherapy (CERs / RTE) requires, before starting to be used clinically in patients undergoing a process of commissioning dosimetry, which evaluates all geometric parameters, physical, Dosimetric and technical impact on the precision and accuracy of treatment to administer, and therefore its effectiveness. This process includes training and familiarization of the multidisciplinary team (medical physicists, radiation oncologists, neurosurgeons, dosimetrists, biomedical engineers) with the equipment and techniques used, the quality assurance program and special radiation protection standards for this technology. The aim of this work is to prepare the pre-clinical dosimetric conditions to ensure the quality and radiation safety of treatment with CER RTE. Treatment with CER RTE INOR has a linear accelerator equipped with a micro-multileaf collimator dynamic tertiary (dMLC 3Dline). The system aceleradordMLC geometric and dosimetric was calibrated, using ionization chambers miniature, diode and film dosimetry. The immobilization of the patient and location of the lesion is made by both invasive stereotactic frames and relocatable. The computerized planning of the CER / TEN is done with the ERGO system, for which commissioning is designed test cases of increasing complexity, using planes and anthropomorphic dummies, which help assess the accuracy of the dosimetric calculations and accuracy of the system as a whole. We compared the results of the planning system with measurements, showing that the discrepancies are within tolerances, so it is concluded that from the standpoint of physical dosimetry, the system-under-ERGO accelerator MLC is eligible for clinical use. (author)