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Order No. 17-N of the Ministry of Public Health validating Sanitary and hygienic requirements for disinfectants, insecticides and hazardous substances No. 2.1.7.006-14.

País/Territorio
Armenia
Tipo de documento
Reglamento
Fecha
2014
Fuente
FAO, FAOLEX
Materia
Agricultura y desarrollo rural, Medio ambiente gen., Cultivos
Palabra clave
Desinfección/desinfestación Agentes de control biológico Salud pública Sustancias peligrosas Monitoreo Toxicidad/envenenamiento Envasado/etiquetado
Área geográphica
Asia, CEI (Comunidad de Estados Independientes), Europa, Europa y Central Asia, Naciones en desarrollo sin litoral, Asia Occidental
Entry into force notes
This Order enters into force on 11 July 2014.
Resumen

These requirements apply to insecticides, antioxidants, disinfectants and other similar substances packed in containers or in packages for retail trade, or ready-made preparations or products that are designed for everyday life-time medical care for use in organizations providing assistance and service, and other facilities, ensuring the safety of human life and health. The criteria for the safety assessment of substances affecting disinfectants shall be as follows: (a) acute, subacute, chronic toxicity, including the effects on human health and individual effects assessment (allergen, reproductive toxicity, teratogenicity, mutagenicity, carcinogenicity, embryo); (b) technical products of the registered disinfectant (substance, the affected substances); (c) compliance with the technical product of the manufacturer; (d) hazardous (toxicological) mixtures of technical products; (e) availability of metabolites; (f) hygienic standards of the affected substances in the working zones, atmospheric air in the residential areas, the content of substances in water and soil of the reservoirs and the environment; with the use of monitoring data (if available). Preparation of microorganisms (bacteria) production stages and ready-made forms of biofuels, evaluation criteria shall be as follows: (a) conditions of origin and cultivation, the method of identifying it, strain distribution; (b) pathogens of bacteria (virality, toxicity); (c) the irritant effect on the eye mucous membrane; (d) microorganisms' sensitivity and immunotherapeutic effect on the skin or upper respiratory tract infections; and (e) criteria for the limitation of harmfulness during chronic trials.

Texto completo
Armenio
Página web
www.arlis.am