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ANSI/ASSE Z359 Fall Protection Code Package v3.0

ANSI/ASSE Z359 Fall Protection Code Package Version 3.0

The Z359 Fall Protection Code - Version 3.0 package includes ANSI/ASSE Z359.0-2012 - Definitions and Nomenclature Used for Fall Protection and Fall Arrest ANSI/ASSE Z359.1-2016 - Safety Requirements for Personal Fall Arrest Systems, Subsystems and Components ANSI/ASSE Z359.2-2017 - Minimum Requirements for a Comprehensive Managed Fall Protection Program ANSI/ASSE Z359.3-2017 - Safety Requirements for Positioning and Travel Restraint Systems ANSI/ASSE Z359.4-2013 - Safety Requirements for Assisted-Rescue and Self-Rescue Systems, Subsystems and Components ANSI/ASSE Z359.6-2016 - Specifications and Design Requirements for Active Fall Protection Systems ANSI/ASSE Z359.7-2011 - Qualification and Verification Testing of Fall Protection Products ANSI/ASSE Z359.11-2014 - Safety Requirements for Full Body Harnesses ANSI/ASSE Z359.12-2009 - Connecting Components for Personal Fall Arrest System ANSI/ASSE Z359.13-2013 - Personal Energy Absorbers and Energy Absorbing Lanyards ANSI/ASSE Z359.14-2014 - Safety Requirements for Self-Retracting Devices For Personal Fall Arrest and Rescue Systems ANSI/ASSE Z359.15-2014 - Safety Requirements for Single Anchor Lifelines and Fall Arresters for Personal Fall Arrest and Rescue Systems ANSI/ASSE Z359.16-2016 - Safety Requirements for Climbing Ladder Fall Arrest Systems ANSI/ASSE Z359.18-2017 - Safety Requirements for Anchorage Connectors for Active Fall Protection Systems - Part of the Fall Protection Code Reference Standards and Documents ANSI/ASSE Z359.1-1992 (R1999) - Historical Document ANSI/ASSE A10.32-2012 ANSI/ASSE Z490.1-2016


ANSI/ISEA Z358.1-2014

American National Standard for Emergency Eyewash and Shower Equipment

This standard establishes minimum performance and use requirements for eyewash and shower equipment for the emergency treatment of the eyes or body of a person who has been exposed to hazardous materials. It covers the following types of equipment: emergency showers, eyewashes, eye/face washes, and combination units. This standard also includes performance and use requirements for personal wash units and drench hoses, which are considered supplemental to emergency eyewash and shower equipment.


ISO/IEC 17025:2017

General requirements for the competence of testing and calibration laboratories

ISO/IEC 17025:2017 specifies the general requirements for the competence, impartiality and consistent operation of laboratories. ISO/IEC 17025:2017 is applicable to all organizations performing laboratory activities, regardless of the number of personnel. Laboratory customers, regulatory authorities, organizations and schemes using peer-assessment, accreditation bodies, and others use ISO/IEC 17025:2017 in confirming or recognizing the competence of laboratories.


ISO 9001:2015

Quality management systems - Requirements

ISO 9001:2015 specifies requirements for a quality management system when an organization: a) needs to demonstrate its ability to consistently provide products and services that meet customer and applicable statutory and regulatory requirements, and b) aims to enhance customer satisfaction through the effective application of the system, including processes for improvement of the system and the assurance of conformity to customer and applicable statutory and regulatory requirements. All the requirements of ISO 9001:2015 are generic and are intended to be applicable to any organization, regardless of its type or size, or the products and services it provides.

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ISO/IEC 27001:2013

Information technology - Security techniques - Information security management systems - Requirements

ISO/IEC 27001:2013 specifies the requirements for establishing, implementing, maintaining and continually improving an information security management system within the context of the organization. It also includes requirements for the assessment and treatment of information security risks tailored to the needs of the organization. The requirements set out in ISO/IEC 27001:2013 are generic and are intended to be applicable to all organizations, regardless of type, size or nature.


ISO 45001:2018

Occupational health and safety management systems - Requirements with guidance for use

ISO 45001:2018 specifies requirements for an occupational health and safety (OH b) fulfilment of legal requirements and other requirements; c) achievement of OH&S objectives. ISO 45001:2018 is applicable to any organization regardless of its size, type and activities. It is applicable to the OH&S risks under the organization's control, taking into account factors such as the context in which the organization operates and the needs and expectations of its workers and other interested parties. ISO 45001:2018 does not state specific criteria for OH&S performance, nor is it prescriptive about the design of an OH&S management system. ISO 45001:2018 enables an organization, through its OH&S management system, to integrate other aspects of health and safety, such as worker wellness/wellbeing. ISO 45001:2018 does not address issues such as product safety, property damage or environmental impacts, beyond the risks to workers and other relevant interested parties. ISO 45001:2018 can be used in whole or in part to systematically improve occupational health and safety management. However, claims of conformity to this document are not acceptable unless all its requirements are incorporated into an organization's OH&S management system and fulfilled without exclusion.



ISO 14001:2015

Environmental management systems - Requirements with guidance for use

ISO 14001:2015 specifies the requirements for an environmental management system that an organization can use to enhance its environmental performance. ISO 14001:2015 is intended for use by an organization seeking to manage its environmental responsibilities in a systematic manner that contributes to the environmental pillar of sustainability. ISO 14001:2015 helps an organization achieve the intended outcomes of its environmental management system, which provide value for the environment, the organization itself and interested parties. Consistent with the organization's environmental policy, the intended outcomes of an environmental management system include: + enhancement of environmental performance; + fulfillment of compliance obligations; + achievement of environmental objectives. ISO 14001:2015 is applicable to any organization, regardless of size, type and nature, and applies to the environmental aspects of its activities, products and services that the organization determines it can either control or influence considering a life cycle perspective. ISO 14001:2015 does not state specific environmental performance criteria. ISO 14001:2015 can be used in whole or in part to systematically improve environmental management. Claims of conformity to ISO 14001:2015, however, are not acceptable unless all its requirements are incorporated into an organization's environmental management system and fulfilled without exclusion.

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ISO 10993-1:2018

Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process

This document specifies: the general principles governing the biological evaluation of medical devices within a risk management process; the general categorization of medical devices based on the nature and duration of their contact with the body; the evaluation of existing relevant data from all sources; the identification of gaps in the available data set on the basis of a risk analysis; the identification of additional data sets necessary to analyse the biological safety of the medical device; the assessment of the biological safety of the medical device. This document applies to evaluation of materials and medical devices that are expected to have direct or indirect contact with: the patient's body during intended use; the user's body, if the medical device is intended for protection (e.g., surgical gloves, masks and others). This document is applicable to biological evaluation of all types of medical devices including active, non-active, implantable and non-implantable medical devices. This document also gives guidelines for the assessment of biological hazards arising from: risks, such as changes to the medical device over time, as a part of the overall biological safety assessment; breakage of a medical device or medical device component which exposes body tissue to new or novel materials. Other parts of ISO 10993 cover specific aspects of biological assessments and related tests. Device-specific or product standards address mechanical testing. This document excludes hazards related to bacteria, moulds, yeasts, viruses, transmissible spongiform encephalopathy (TSE) agents and other pathogens.


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As the voice of the U.S. standards and conformity assessment system, the American National Standards Institute (ANSI) empowers its members and constituents to strengthen the U.S. marketplace position in the global economy while helping to assure the safety and health of consumers and the protection of the environment.

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