• Z305.0-13

    Current The latest, up-to-date edition.

    Safety of personnel in perioperative environments

    Available format(s):  Hardcopy, PDF

    Language(s):  English

    Published date:  01-01-2013

    Publisher:  Canadian Standards Association

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    Table of Contents - (Show below) - (Hide below)

    Preface
    0 Introduction
    1 Scope
    2 Reference publications
    3 Definitions
    4 Quality management systems (QMS)
    5 Evaluation and purchase of medical devices used in
       a perioperative environment
    6 Personnel
    7 OHS
    8 Infection prevention and control
    9 Respectful workplace dynamics
    10 Area design and use

    Abstract - (Show below) - (Hide below)

    Overview Perioperative environments and their associated risks are not only found in traditional acute care hospitals but are increasingly common in vision correction, dental offices and other health care settings. From medical devices to chemical and anesthetic agents, the new CSA Z305.0 Safety in Perioperative Environments provides organizations with systematic guidelines to develop and continuously improve safety. Highlights of Z305.0-13 Include: Includes requirements for a quality management system (QMS) that addresses personnel safety, personnel qualifications & training, occupational health & safety and infection prevention & control A focus on hazards and risks associated with perioperative environments Guidance on appropriate policies and procedures Covers medical devices, chemical and anesthetic agents, and team risks

    Scope - (Show below) - (Hide below)

    Preface This is the first edition of CSA Z305.0, Safety of personnel in perioperative environments. Scope 1.1 This Standard includes requirements for a quality management system (QMS) that addresses safety of personnel in perioperative environments including requirements for a) establishing a QMS b) OHS c) policies and SOPs, clinical practice standards, and documentation d) personnel qualifications and training e) work areas and equipment f) infection, prevention, and control g) evaluation and purchase of reusable medical devices 1.2 In this Standard, \"shall\" is used to express a requirement, i.e., a provision that the user is obliged to satisfy in order to comply with the standard; \"should\" is used to express a recommendation or that which is advised but not required; and \"may\" is used to express an option or that which is permissible within the limits of the standard. Notes accompanying clauses do not include requirements or alternative requirements; the purpose of a note accompanying a clause is to separate from the text explanatory or informative material. Notes to tables and figures are considered part of the table or figure and may be written as requirements. Annexes are designated normative (mandatory) or informative (non-mandatory) to define their application.

    General Product Information - (Show below) - (Hide below)

    Document Type Standard
    Publisher Canadian Standards Association
    Status Current

    Standards Referencing This Book - (Show below) - (Hide below)

    CSA Z305.13 : 2013(R2018) PLUME SCAVENGING IN SURGICAL, DIAGNOSTIC, THERAPEUTIC, AND AESTHETIC SETTINGS
    CSA Z317.2 : 2010 SPECIAL REQUIREMENTS FOR HEATING, VENTILATION, AND AIR-CONDITIONING (HVAC) SYSTEMS IN HEALTH CARE FACILITIES
    Z7396.1-17 Medical gas pipeline systems - Part 1: Pipelines for medical gases, medical vacuum, medical support gases, and anaesthetic gas scavenging systems
    CSA Z317.10 : 2015 HANDLING OF HEALTH CARE WASTE MATERIALS
    CSA Z314.22 : 2016 MANAGEMENT OF LOANED, REUSABLE MEDICAL DEVICES
    CSA Z386:2014(R2019) SAFE USE OF LASERS IN HEALTH CARE
    CSA ISO 9001 : 2016 QUALITY MANAGEMENT SYSTEMS - REQUIREMENTS
    CSA Z1000 : 2014 OCCUPATIONAL HEALTH AND SAFETY MANAGEMENT
    CSA ISO 9000 : 2016 QUALITY MANAGEMENT SYSTEMS - FUNDAMENTALS AND VOCABULARY
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