“…In the research byFonseca (2012), the incidence of exposure to biological risks occurs during the procedure with the squirting or sneezing of biological material, in the handling of disposal boxes or even by the recapping of needles, considering that the resurfacing of needles is against biosafety standards(ANVISA, 2005).In relation to operation, according to the literature there is a considerable amount of inadequacies, with a failure in inspections. The research carried out byAraújo Filho et al, (2016) andSimonetti (2014), report failures in the laboratory facilities in which participated in their studies, because these are related to inspection of health surveillance inspectors, with the Programs (PPRA), (PCMSO), (PGRSS), (POPs), with a lack and/or updating of specific SOP, employees who do not know these programs and procedures, who did not receive specific training before starting their activities, work alone in level 3 environments, which is prohibited by Anvisa, lack of accident notification documents, lack of monitoring of professionals intended for cleaning the laboratory, lack of clinical examinations, immunizations And storage of base serum as a control Lima et al, (2016),. notes in his research laboratories with failures in the identification of the establishment, human resources, equipment, waste disposal, biosafety, operational processes, cleaning and quality control, work outside all the standards required by Anvisa, without a sanitary license, technical responsible, professional without proper registration with the equivalent council and…”