Clinical Functionality Sample Clauses
The Clinical Functionality clause defines the required capabilities and performance standards of a product or service within a clinical or healthcare setting. It typically outlines specific features, workflows, or interoperability requirements that the product must support to be effectively used by healthcare professionals, such as electronic health record integration or compliance with clinical protocols. This clause ensures that the delivered solution meets the practical needs of clinical users, thereby reducing the risk of operational inefficiencies or non-compliance with healthcare regulations.
Clinical Functionality. (a) SJHC confirms that, as at the date of this Project Agreement, it has reviewed the Sites master plan, and blocking and stacking diagrams and interdepartmental matrix and that, subject to any qualifications or comments noted thereon, such Submittals satisfy the Output Specifications in respect of Clinical Functionality, so far as can reasonably be determined given the level of detail in the Submittals.
(b) With each of the Design Development Submittals, Project Co shall submit to SJHC, for its review pursuant to Schedule 10 - Review Procedure, a draft report (each a “Clinical Functionality Report”) to specifically identify, with reference to the Output Specifications, such matters of Clinical Functionality that Project Co wishes SJHC to review and consider as part of the Design Development Submittals. Each Clinical Functionality Report shall demonstrate how the Output Specifications are satisfied in respect of Clinical Functionality.
(c) With the Construction Document Submittals, Project Co shall submit to SJHC, for its review pursuant to Schedule 10 - Review Procedure, a final Clinical Functionality Report, and SJHC shall confirm that, subject to any qualifications or comments noted thereon, such Construction Document Submittals satisfy the Output Specifications in respect of Clinical Functionality, so far as can reasonably be determined given the level of detail in the Construction Document Submittals.
(d) Each Clinical Functionality Report must be prepared in accordance with the technical submission requirements set out in MOHLTC’s Capital Planning Manual and must address the way in which the Design Data meets the following requirements of Clinical Functionality:
(i) MOHLTC’s “OASIS” requirements of operational efficiency, accessibility, safety and security, infection prevention and control, and sustainability;
(ii) expansion/ flexibility;
(iii) internal adjacencies;
(iv) internal zoning and material/staff flow;
(v) hours of operation; and
(vi) Plant.
Clinical Functionality. Configuration Issues
Clinical Functionality. Capacity Issues
Clinical Functionality. (a) Contracting Authority confirms that, as at the date of this Project Agreement, it has reviewed the Site master plan and blocking and stacking diagrams and that, subject to any qualifications or comments noted thereon, such Works Submittals satisfy the Output Specifications in respect of Clinical Functionality, so far as can reasonably be determined given the level of detail in the Works Submittals.
Clinical Functionality. Fabric and Infrastructure