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2 Registro/s encontrado/s en CAT+NORMA



Tipo de documento: NORMA
Título: GREENHOUSE GASES -- CARBON FOOTPRINT OF PRODUCTS -- REQUIREMENTS AND GUIDELINES FOR QUANTIFICATION AND COMMUNICATION
Código de Doc.: ISO/TS 14067
Autor Inst.: International Organization for Standardization. ISO
Fecha: 2013
Estado: Para datos sobre la vigencia de esta norma haga clic aquí
Objeto: ISO/TS 14067:2013 specifies principles, requirements and guidelines for the quantification and communication of the carbon footprint of a product (CFP), based on International Standards on life cycle assessment (ISO 14040 and ISO 14044) for quantification and on environmental labels and declarations (ISO 14020, ISO 14024 and ISO 14025) for communication. Requirements and guidelines for the quantification and communication of a partial carbon footprint of a product (partial CFP) are also provided
Campo de Aplic.: ISO/TS 14067:2013 is applicable to CFP studies and different options for CFP communication based on the results of such studies. Where the results of a CFP study are reported according to ISO/TS 14067:2013, procedures are provided to support both transparency and credibility and also to allow for informed choices. ISO/TS 14067:2013 also provides for the development of CFP-product category rules (CFP-PCR), or the adoption of product category rules (PCR) that have been developed in accordance with ISO 14025 and that are consistent with ISO/TS 14067:2013. ISO/TS 14067:2013 addresses only one impact category: climate change
ICS: 13.020.40
Idioma: en
Título en otro Idioma: Gaz à effet de serre -- Empreinte carbone des produits - Exigences et lignes directrices pour la quantification et la communication
Edición: first edition
Palabras Clave: Gases; Efecto invernadero; Huella de carbono; Productos; Huella ecológica; Requisitos; Comunicación; Cuantificación
Páginas: 52p.
Ingreso de la Info.: 2015-01-19
Para ver la norma completa busque en la base Normas (solo para personal del INTI)



Tipo de documento: NORMA
Título: BIOLOGICAL EVALUATION OF MEDICAL DEVICES -- PART 13: IDENTIFICATION AND QUANTIFICATION OF DEGRADATION PRODUCTS FROM POLYMERIC MEDICAL DEVICES
Código de Doc.: ISO 10993-13:1998
Autor Inst.: International Organization for Standardization. ISO
Fecha: 1998
Estado: Para datos sobre la vigencia de esta norma haga clic aquí
Objeto: This part of ISO 10993 provides guidance on general requirements for the design of tests for identifying and quantifying degradation products from finished polymeric medical devices ready for clinical use. This part of ISO 10993 describes two test methods to generate degradation products, an accelerated degradation test as a screening method and a real-time degradation test. For materials which are intended to polymerize in situ, the set or cured polymer is used for testing. The data generated are used in the biological evaluation of the polymer. This part of ISO 10993 considers only those degradation products generated by a chemical alteration of the finished polymeric device. It is not applicable to degradation of the device induced during its intended use by mechanical stress, wear or electromagnetic radiation. The biological activity of the debris and soluble degradation products is not addressed in this part of ISO 10993, but should be evaluated according to the principles of ISO 10993-1 and ISO 14538. Because of the wide range of polymeric materials used in medical devices, no specific analytical techniques are identified or given preference. No specific requirements for acceptable levels of degradation products are provided in this part of ISO 10993
Relac. con otras Normas: ISO 10993-1; ISO 10993-2; ISO 10993-3; ISO 10993-4; ISO 10993-5; ISO 10993-6; ISO 10993-7; ISO 10993-9; ISO 10993-10; ISO 10993-11; ISO 10993-12
ICS: 11.100.20
Idioma: en
Título en otro Idioma: Evaluation biologique des dispositifs médicaux -- Partie 13: Identification et quantification de produits de dégradation de dispositifs médicaux a base de polymere
Edición: first edition
Notas: Revised by: ISO/DIS 10993-13
Palabras Clave: Evaluación biologica; Dispositivos médicos; Polímeros; Ensayos; Identificación; Cuantificación; Productos de degradación
Páginas: 10p.
Ingreso de la Info.: 2009-08-26
Para ver la norma completa busque en la base Normas (solo para personal del INTI)



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