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INFORMATION TECHNOLOGY - SECURITY TECHNIQUES - EVALUATION CRITERIA FOR IT SECURITY - PART 3: SECURITY ASSURANCE COMPONENTS (SECOND REVISION) (ISO/IEC 15408-3:2008, IDT)
MS ISO/IEC 15408-3:2010
Status : 2nd Revision
Format : PDF

This Malaysian Standard defines the assurance requirements of ISO/IEC 15408. It includes the evaluation assurance levels (EALs) that define a scale for measuring assurance for component TOEs, the comp ....Read more osed assurance packages (CAPs) that define a scale for measuring assurance for composed TOEs, the individual assurance components from which the assurance levels and packages are composed, and the criteria for evaluation of PPs and STs. Close

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INFORMATION TECHNOLOGY - SECURITY TECHNIQUES - EVALUATION CRITERIA FOR IT SECURITY - PART 2: SECURITY FUNCTIONAL REQUIREMENTS(FIRST REVISION)(ISO/IEC 15408-2:2005, IDT)
MS ISO/IEC 15408-2:2005
Status : 1st Revision
Format : PDF

This Malaysian Standard defines the required structure and content of security functional components for the purpose of security evaluation. It includes a catalogue of functional components that will ....Read more meet the common security functionality requirements of many IT products and systems. Close

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INFORMATION TECHNOLOGY - SECURITY TECHNIQUES - EVALUATION CRITERIA FOR IT SECURITY - PART 1: INTRODUCTION AND GENERAL MODEL (FIRST REVISION)(ISO/IEC 15408-1:2005, IDT)
MS ISO/IEC 15408-1:2005
Status : 1st Revision
Format : PDF

This Malaysian Standard defines two forms for expressing IT security functional and assurance requirements. The protection profile (PP) construct allows creation of generalized reusable sets of these ....Read more security requirements. The PP can be used by prospective consumers for specification and identification of products with IT security features which will meet their needs. The security target (ST) expresses the security requirements and specifies the security functions for a particular product or system to be evaluated, called the target of evaluation (TOE). The ST is used by evaluators as the basis for evaluations conducted in accordance with MS ISO/IEC 15408. Close

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Protective gloves for firefighters - laboratory test methods and performance requirements (ISO 15383:2001, IDT)
MS ISO 15383:2005 (CONFIRMED:2012)
Status : 1st Confirmation
Format : PDF

This Malaysian Standard specifies test methods and minimum requirements for protective gloves to be worn during firefighting and associated activities where there is a risk of heat and/or flame.
....Read more >
The purpose of this standard is to provide minimum performance requirements for protective gloves designed to protect against injury in fire fighting operations. Close

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Pulp, paper and board - Determination of pentachlorophenol in an aqueous extract (ISO 15320:2011, IDT)
MS ISO 15320:2012 (CONFIRMED:2023)
Status : 1st Confirmation
Format : PDF

This Malaysian Standard specifies a test method for the determination of pentachlorophenol (PCP) in an aqueous extract of pulp, paper and board. Although it was developed for paper and board intended ....Read more to come into contact with foodstuffs, it is applicable to all kinds of pulp, paper and board.

The working range for acetylation is 0,05 mg/kg to 0,5 mg/kg.

NOTE The upper limit of the working range could be increased if the aqueous extract is diluted. Close

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ANIMAL AND VEGETABLE FATS AND OILS – DETECTION AND IDENTIFICATION OF A VOLATILE ONRGANIC CONTAMINANT BY GC/MS (ISO 15303:2001, IDT)
MS ISO 15303:2007
Status : Original
Format : PDF

This Malaysian Standard specifies a method for the detection and identification of a volatile organic contaminantin edible oils.

It is applicable to the identification of volatile indust ....Read more rial chemicals in both crude and refined edible oils that are suspected of being contaminated. It also enables determination of the concentration of the contaminant.

This Malaysian Standard is not applicable to the determination of the concentration of chemicals that may react with the edible oil or with one of its natural components. In these cases, the presence of the contaminant may sometimes be established on a qualitative basis. Also, this International Standard is not applicable to non-volatile chemicals.

This Malaysian Standard has been shown to be applicable for the identification of the following compound classes:
- saturated halogenated hydrocarbons;
- unsaturated halogenated hydrocarbons;
- esters; aldehydes; alcohols; amines; ketones; ethers;
- cyclic and aromatic compounds; Close

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PLASTICS - GUIDELINES FOR THE RECOVERY AND RECYCLING OF PLASTICS WASTE (ISO 15270:2008, IDT)
MS ISO 15270:2008
Status : Original
Format : PDF

This Malaysian Standard provides guidance for the development of standards and specifications covering plastics waste recovery, including recycling. The standard establishes the different options for ....Read more the recovery of plastics waste arising from pre-consumer and post-consumer sources as illustrated diagrammatically in Annex A. The standard also establishes the quality requirements that should be considered in all steps of the recovery process, and provides general recommendations for inclusion in material standards, test standards and product specifications. Consequently, the process stages, requirements, recommendations and terminology presented in this International Standard are intended to be of general applicability. Close

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Ergonomics of the thermal environment - Risk assessment strategy for the prevention of stress or discomfort in thermal working conditions (ISO 15265:2004, IDT)
MS ISO 15265:2008 (CONFIRMED:2019)
Status : 1st Confirmation
Format : PDF

This Malaysian Standard describes a strategy for assessing and interpreting the risk of physiological constraints, or of discomfort, while working in a given climatic environment.

It is ....Read more applicable in any working situation with steady or varying conditions of the climate, metabolic rate or clothing.

This Malaysian Standard does not describe a single procedure, but a strategy in three stages that can be used successively to gain deeper insight in the working conditions, as it is needed to draw the most appropriate conclusions about the risk involved and identify the best control and prevention measures.

It is definitely oriented towards the prevention and/or control of these working problems in the heat or cold. The risk of heat or cold disorders and/or discomfort is therefore assessed only to the extent that it is required to reach this goal.

However, users must comply with national legislations that may require that risk assessment be performed more systematically.

As the st Close

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Medical devices - Quality management - Medical device nomenclature data structure (First Revision) (ISO 15225:2010, IDT)
MS ISO 15225:2011
Status : Withdrawn
Format : PDF

This Malaysian Standard provides rules and guidelines for a medical device nomenclature data structure, in order to facilitate cooperation and exchange of data used by regulatory bodies on an internat ....Read more ional level between interested parties, e.g. regulatory authorities, manufacturers, suppliers, health care providers and end users.

This standard includes guidelines for a minimum data set and its structure. These guidelines are provided for system designers setting up databases that utilize the nomenclature system described herein.

The requirements contained in this standard are applicable to the development and maintenance of an international nomenclature for medical device identification.

This standard does not include the nomenclature itself, which is provided as a data file. Close

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Clinical laboratory medicine - In vitro diagnostic medical devices - Validation of user quality control procedures by the manufacturer (ISO 15198:2004, IDT)
MS ISO 15198:2008 (CONFIRMED:2015)
Status : Withdrawn
Format : PDF

This Malaysian Standard describes a process for manufacturers of in vitro diagnostic medical devices to validate quality control procedures they recommend to their users. These quality control procedu ....Read more res are intended to provide users with assurance that device performance is consistent with its intended use and the manufacturers' claims. This standard applies to all in vitro diagnostic medical devices. Close

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