Common use of Clinical Functionality Clause in Contracts

Clinical Functionality. (a) NHS confirms that, as at the date of this Project Agreement, it has reviewed the Site master plan, 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 NHS, 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 NHS 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 NHS, for its review pursuant to Schedule 10 - Review Procedure, a final Clinical Functionality Report, and NHS 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, accessibly, 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. (a) NHS WCH confirms that, as at the date of this Project Agreement, it has reviewed the Site 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 NHSWCH, 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 NHS WCH 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 NHSWCH, for its review pursuant to Schedule 10 - Review Procedure, a final Clinical Functionality Report, and NHS WCH 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 ’s Capital Planning Manual and must address the way in which the Design Data meets the following requirements of Clinical Functionality: (i) MOHLTC's "’s “OASIS" ” requirements of operational efficiency, accessiblyaccessibility, 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. (a) NHS CAMH confirms that, as at the date of this Project Agreement, it has reviewed the Site master plan, 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 NHSCAMH, 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 NHS CAMH 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 NHSCAMH, for its review pursuant to Schedule 10 - Review Procedure, a final Clinical Functionality Report, and NHS CAMH 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 ’s Capital Planning Manual and must address the way in which the Design Data meets the following requirements of Clinical Functionality: (i) MOHLTC's "’s “OASIS" ” requirements of operational efficiency, accessiblyaccessibility, 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. (a) NHS Contracting Authority confirms that, as at the date of this Project Agreement, it has reviewed the Site master plan, plan and blocking and stacking diagrams and interdepartmental matrix 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. (b) With each of the Design Development Submittals, Project Co shall submit to NHSContracting Authority, 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 NHS Contracting Authority 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 NHSContracting Authority, for its review pursuant to Schedule 10 - – Review Procedure, a final Clinical Functionality Report, and NHS Contracting Authority 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 the Output Specifications and Schedule 10 – Review Procedure. Each Clinical Functionality Report must address the way in which the Design Data meets the following requirements of Clinical Functionality: (i) MOHLTC's "OASIS" requirements of operational efficiency, accessiblyaccessibility, safety and security, infection prevention and control, and sustainability, as specified in the Output Specifications, including and in particular, meeting the design requirement for functional program accommodation along with accessibility, furniture, fixture, and equipment requirements; (ii) expansion/ flexibility; (iii) internal adjacencies; (iv) internal zoning and material/staff flow; (v) hours of operationspace variance; (vi) work sequencing to maintain Contracting Authority Activities on a 24/7 basis; and (vivii) Planthours of operation.

Clinical Functionality. (a) NHS SJHC confirms that, as at the date of this Project Agreement, it has reviewed the Site 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 NHSSJHC, 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 NHS 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 NHSSJHC, for its review pursuant to Schedule 10 - Review Procedure, a final Clinical Functionality Report, and NHS 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 ’s Capital Planning Manual and must address the way in which the Design Data meets the following requirements of Clinical Functionality: (i) MOHLTC's "’s “OASIS" ” requirements of operational efficiency, accessiblyaccessibility, 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. (a) NHS Contracting Authority confirms that, as at the date of this Project Agreement, it has reviewed the Site master plan, plan and blocking and stacking diagrams and interdepartmental matrix 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. (b) With each of the Design Development Submittals, Project Co shall submit to NHSContracting Authority, 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 NHS Contracting Authority 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 NHSContracting Authority, for its review pursuant to Schedule 10 - – Review Procedure, a final Clinical Functionality Report, and NHS Contracting Authority 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 MOH’s “Capital Planning Manual Manual” and must address the way in which the Design Data meets the following requirements of Clinical Functionality: (i) MOHLTC's "MOH’s “OASIS" ” requirements of operational efficiency, accessiblyaccessibility, 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 operationspace variance; (vi) phasing and decanting approach; and (vivii) Planthours of operation.

Clinical Functionality. (a) NHS SMH confirms that, as at the date of this Project Agreement, it has reviewed the Site master plan, plan and blocking and stacking diagrams and interdepartmental matrix 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. (b) With each of the Design Development Submittals, Project Co shall submit to NHSSMH, 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 NHS SMH 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 NHSSMH, for its review pursuant to Schedule 10 - – Review Procedure, a final Clinical Functionality Report, and NHS SMH 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 ’s “Capital Planning Manual Manual” and must address the way in which the Design Data meets the following requirements of Clinical Functionality: (i) MOHLTC's "’s “OASIS" ” requirements of operational efficiency, accessiblyaccessibility, 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) the Plant.

Clinical Functionality. (ax) NHS Xxxxx confirms that, as at the date of this Project Agreement, it has reviewed the Site master plan, and blocking and stacking diagrams and interdepartmental matrix submitted by Project Co 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 NHSXxxxx, 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 NHS Xxxxx 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 NHSOsler, for its review pursuant to Schedule 10 - – Review Procedure, a final Clinical Functionality Report, and NHS Xxxxx 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 ’s Capital Planning Manual and must address the way in which the Design Data meets the following requirements of Clinical Functionality: (i) MOHLTC's "’s “OASIS" ” requirements of operational efficiency, accessiblyaccessibility, safety and security, infection prevention and control, and sustainability; (ii) expansion/ expansion/flexibility; (iii) internal adjacencies; (iv) internal zoning and material/staff flow; (v) hours of operation; and (vi) Plant.

Clinical Functionality. (a) NHS HRRH confirms that, as at the date of this Project Agreement, it has reviewed the Site 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 NHSHRRH, 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 NHS HRRH 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 NHSHRRH, for its review pursuant to Schedule 10 - Review Procedure, a final Clinical Functionality Report, and NHS HRRH 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 ’s Capital Planning Manual and must address the way in which the Design Data meets the following requirements of Clinical Functionality: (i) MOHLTC's "’s “OASIS" ” requirements of operational efficiency, accessiblyaccessibility, 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. (a) NHS JBH confirms that, as at the date of this Project Agreement, it has reviewed the Site master plan, plan and blocking and stacking diagrams and interdepartmental matrix 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. (b) With each of the Design Development Submittals, Project Co shall submit to NHSJBH, 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 NHS JBH 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 NHSJBH, for its review pursuant to Schedule 10 - – Review Procedure, a final Clinical Functionality Report, and NHS JBH 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 ’s “Capital Planning Manual Manual” and must address the way in which the Design Data meets the following requirements of Clinical Functionality: (i) MOHLTC's "’s “OASIS" ” requirements of operational efficiency, accessiblyaccessibility, 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 operationspace variance; (vi) phasing and decanting approach; and (vivii) Planthours of operation.

Clinical Functionality. (a) NHS HHS confirms that, as at the date of this Project Agreement, it has reviewed the Site 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 NHSHHS, 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 NHS HHS 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 NHSHHS, for its review pursuant to Schedule 10 - Review Procedure, a final Clinical Functionality Report, and NHS HHS 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 ’s Capital Planning Manual and must address the way in which the Design Data meets the following requirements of Clinical Functionality: (i) MOHLTC's "’s “OASIS" ” requirements of operational efficiency, accessiblyaccessibility, 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. (a) NHS Contracting Authority confirms that, as at the date of this Project Agreement, it has reviewed the Site master plan, plan and blocking and stacking diagrams and interdepartmental matrix 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. (b) With each of the Design Development Submittals, Project Co shall submit to NHSContracting Authority, 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 NHS Contracting Authority 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 NHSContracting Authority, for its review pursuant to Schedule 10 - – Review Procedure, a final Clinical Functionality Report, and NHS Contracting Authority 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 ’s “Capital Planning Manual Manual” and must address the way in which the Design Data meets the following requirements of Clinical Functionality: (i) MOHLTC's "’s “OASIS" ” requirements of operational efficiency, accessiblyaccessibility, safety and security, infection prevention and control, and sustainability; (ii) expansion/ flexibility; (iii) internal adjacencies; (iv) internal zoning and material/staff flow; (v) space variance; (vi) phasing and decanting approach; (vii) hours of operation; and (viviii) the Plant.