Operation and maintenance of health care facilities

Designation Number:
Z8002
Standard Type:
National Standard of Canada - Domestic
Standard Development Activity:
New Edition
ICS code(s):
11.020
Status:
Proceeding to development
SDO Comment Period Start Date:
SDO Comment Period End Date:
Posted On:

Scope:

Scope

Note: The scope of this Notice of Intent (originally published on March 26, 2024) was updated by the responsible SDO on September 4, 2024.

 

1 Scope

1.1 Requirements for operation and maintenance of HCFs

This Standard describes the requirements, including quality system requirements, for the O&M of a HCF. It sets out specific requirements for

a) facility architectural systems; 

b) exterior site elements related to the building and its functions; 

c)  utilities; 

d) the facility’s infrastructure, including but not limited to mechanical, electrical, and information management and information technology, and security systems; 

e) health care equipment;

f) life safety systems; 

g)  specialized functional programs, including but not limited to ORs, MDR, pharmacy, and laboratories; 

h) permanently installed equipment as specified in Clause 1.4;

i) building services and interfaces for installed equipment, both medical and non-medical; and 

j) best practices for sustainability, resilience, energy conservation, decarbonization and adaptation to climate change

Note: The HCF should be aware of federal, provincial/territorial, and municipal regulatory requirements applying to O&M and life safety systems, in addition to relevant CSA Group standards.

1.2 Establishing requirements for HCFs

This Standard establishes requirements for the HCF as a whole.

Note: HCFs vary widely in size, scope, and organization. This Standard sets out the essential O&M requirements for an HCF: it is expected that the HCF will develop the appropriate administrative structures and reporting relationships.

1.3 Organization and coordination with other departments in O&M activities

This Standard addresses the organization of, and the policies and procedures regarding other departments as they relate to O&M activities. It also includes requirements for the necessary coordination of O&M activities with other related HCF departments and functions.

Note: Examples of other departments and functions include security, biomedical engineering, environmental services, housekeeping, and nursing.

1.4 O&M of patient care equipment and interfaces

This Standard addresses the operation and maintenance of permanently installed equipment used to support patient care (e.g., call systems, human waste disposal units). It also includes requirements for the O&M of interfaces between equipment and building systems (e.g., equipment docking and charging stations).

Notes:

1) There is not always a clear line between the services and interfaces that support clinical equipment [see Clause 1.1, Item g)], and the clinical equipment itself. At a minimum, interfaces include physical space requirements and the use of utilities; however, there can be other connections (e.g., mechanical, electrical, computerization, telemetry, etc.). Problems can arise when different departments of the HCF each assume that the other is looking after a particular system. Among the tasks involved in planning an O&M program are to determine where the divisions are and then to document who is responsible for the different elements of the system.

2) In smaller facilities, O&M personnel or a department could have responsibility for equipment maintenance beyond the scope of this Standard. In that case, the person or department responsible for O&M should develop the appropriate expertise and consult relevant standards for these expanded duties (e.g., standards for biomedical engineering).

1.5 Non-assignment of responsibilities to specific job titles or departments

This Standard does not assign responsibilities to specific job titles or departments.

1.6 Exclusions

This Standard does not address the operation and maintenance of clinical equipment used for life support or therapeutic purposes (e.g., infusion pumps, anaesthetic workstations, and MRI machines).

1.7 Interpretation of terms and annex designation

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 (nonmandatory) to define their application.

Project need:

Project Need

To update the current standard due to user experience/feedback/new technology (new edition). This proposed New Edition is being developed at the request of members and stakeholders. It will provide the industry with updated information for operating and maintain a health care facility in Canada.

Note: The information provided above was obtained by the Standards Council of Canada (SCC) and is provided as part of a centralized, transparent notification system for new standards development. The system allows SCC-accredited Standards Development Organizations (SDOs), and members of the public, to be informed of new work in Canadian standards development, and allows SCC-accredited SDOs to identify and resolve potential duplication of standards and effort.

Individual SDOs are responsible for the content and accuracy of the information presented here. The text is presented in the language in which it was provided to SCC.