Common use of Clinical Functionality Clause in Contracts

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. (a) SJHC HHS confirms that, as at the date of this Project Agreement, it has reviewed the Sites 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 SJHCHHS, 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 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 SJHCHHS, for its review pursuant to Schedule 10 - Review Procedure, a final Clinical Functionality Report, and SJHC 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 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. (a) SJHC NHS confirms that, as at the date of this Project Agreement, it has reviewed the Sites 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 SJHCNHS, 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 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 SJHCNHS, for its review pursuant to Schedule 10 - Review Procedure, a final Clinical Functionality Report, and SJHC 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 '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, accessibilityaccessibly, 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▇) SJHC ▇▇▇▇▇ confirms that, as at the date of this Project Agreement, it has reviewed the Sites 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 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 SJHCOsler, 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/ expansion/flexibility; (iii) internal adjacencies; (iv) internal zoning and material/staff flow; (v) hours of operation; and (vi) Plant.

Clinical Functionality. (a) SJHC CAMH confirms that, as at the date of this Project Agreement, it has reviewed the Sites 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 SJHCCAMH, 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 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 SJHCCAMH, for its review pursuant to Schedule 10 - Review Procedure, a final Clinical Functionality Report, and SJHC 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 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. (a) SJHC SMH confirms that, as at the date of this Project Agreement, it has reviewed the Sites 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 SJHCSMH, 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 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 SJHCSMH, for its review pursuant to Schedule 10 - – Review Procedure, a final Clinical Functionality Report, and SJHC 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 “Capital Planning Manual 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) the Plant.

Clinical Functionality. (a) SJHC JBH confirms that, as at the date of this Project Agreement, it has reviewed the Sites 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 SJHCJBH, 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 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 SJHCJBH, for its review pursuant to Schedule 10 - – Review Procedure, a final Clinical Functionality Report, and SJHC 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 “Capital Planning Manual 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 operationspace variance; (vi) phasing and decanting approach; and (vivii) Planthours of operation.

Clinical Functionality. (a) SJHC Contracting Authority confirms that, as at the date of this Project Agreement, it has reviewed the Sites 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 SJHCContracting 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 SJHC 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 SJHCContracting Authority, for its review pursuant to Schedule 10 - – Review Procedure, a final Clinical Functionality Report, and SJHC 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, accessibility, 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) SJHC HRRH confirms that, as at the date of this Project Agreement, it has reviewed the Sites 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 SJHCHRRH, 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 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 SJHCHRRH, for its review pursuant to Schedule 10 - Review Procedure, a final Clinical Functionality Report, and SJHC 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 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. (a) SJHC Contracting Authority confirms that, as at the date of this Project Agreement, it has reviewed the Sites 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 SJHCContracting 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 SJHC 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 SJHCContracting Authority, for its review pursuant to Schedule 10 - – Review Procedure, a final Clinical Functionality Report, and SJHC 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 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) space variance; (vi) phasing and decanting approach; (vii) hours of operation; and (viviii) the Plant.

Clinical Functionality. (a) SJHC Contracting Authority confirms that, as at the date of this Project Agreement, it has reviewed the Sites 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 SJHCContracting 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 SJHC 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 SJHCContracting Authority, for its review pursuant to Schedule 10 - – Review Procedure, a final Clinical Functionality Report, and SJHC 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 MOHLTCMOH’s “Capital Planning Manual Manual” and must address the way in which the Design Data meets the following requirements of Clinical Functionality: (i) MOHLTCMOH’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 operationspace variance; (vi) phasing and decanting approach; and (vivii) Planthours of operation.

Clinical Functionality. (a) SJHC WCH confirms that, as at the date of this Project Agreement, it has reviewed the Sites 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 SJHCWCH, 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 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 SJHCWCH, for its review pursuant to Schedule 10 - Review Procedure, a final Clinical Functionality Report, and SJHC 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 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.