Citas bibligráficas
Aranibar, A., (2021). Implementación del sistema HACCP para asegurar la inocuidad en la producción del queso paria, de la Empresa Danielita, Cusco, 2019 [Universidad Andina del Cusco]. https://hdl.handle.net/20.500.12557/4174
Aranibar, A., Implementación del sistema HACCP para asegurar la inocuidad en la producción del queso paria, de la Empresa Danielita, Cusco, 2019 []. PE: Universidad Andina del Cusco; 2021. https://hdl.handle.net/20.500.12557/4174
@misc{renati/960246,
title = "Implementación del sistema HACCP para asegurar la inocuidad en la producción del queso paria, de la Empresa Danielita, Cusco, 2019",
author = "Aranibar Aranibar, Andrea Dayana",
publisher = "Universidad Andina del Cusco",
year = "2021"
}
This thesis was carried out with the purpose of implementing the Haccp System to ensure safety in the production of Paria cheese at the Danielita company. With this system it is possible to reduce the amount of microorganisms for the raw material and final product with the help of the identification of latent hazards in the production process and to create a documentation system that accredits constant monitoring, where 11 biological hazards, 4 physical hazards and 3 chemical hazards were found, which have their preventive measure and avoid the contamination of the cheese. The Digesa report identified the level of compliance that the standard requires of the prerequisites for the HACCP system; the company only complied with 23%, obtaining a poor rating, but after the implementation of the prerequisites, it achieved a compliance score of 85% was achieved, obtaining a very good rating, because it developed from scratch the good manufacturing practices manuals with 9 programs, the sanitation standard operating procedures manual with 7 programs and the development of the HACCP plan with its respective formats. The quantity of microorganisms that were reduced in the raw material were mesophilic aerobes, which reduced the microbial load from 150 colony-forming units to 40 colonyforming units, reducing the percentage to 73%; for coliforms, it was reduced from 120 colony-forming units to 17 colony-forming units, reducing the percentage to 86%. For the final product it was possible to reduce the amount of microorganisms, for total coliforms it reduced the microbial load from 570 colony forming units to 280 colony forming units, reducing percentage to 51%, for fecal coliforms it reduced from 360 colony forming units to 160 colony forming units, reducing percentage to 56% and for Escherichia coli it reduced from 280 colony forming units to 0 colony forming units, reducing percentage to 100%.
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