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General Terms and Conditions of Sale and Software License
(“Conditions of Sale”) (Rev 26.1)
Schedule 1
Imaging Systems Portfolio (IS) (Rev 26.1)
| Product Category | Products |
| Image Guided Therapy (IGT) | Interventional X-Ray (iXR) |
| Mobile C-Arms (Surg) | |
| Philips Image Guided Therapy Corporation (IGTD) fka Volcano (capital only) | |
| Diagnostic Imaging | Digital X-Ray (DXR) |
| Computed Tomography (CT) | |
| Magnetic Resonance (MR) | |
| OEM Imaging Components (Coils) | |
| Positron Emission Tomography (PET/CT) | |
| Advanced Molecular Imaging (SPECT & SPECT/CT) | |
| Radiation Oncology (PROS) |
Schedule 1-A
MR Subscription (Rev 26.1)
| Product Category | Products |
| Magnetic Resonance (MR) | MRI Software License Packages |
The following Schedule 1-A shall apply to Magnetic Resonance Software License Packages offered under the MR Subscription.
[ ] Quarterly Basis
[ ] Monthly Basis
[ ] Yearly Basis
[ ] One-Time Advance Payment
Fees for renewals or Subscriptions added during the Term will be at Philips’ current standard price, due at the beginning of the Subscription Term, charged for the full calendar month in which Subscriptions are added, and coterminous with the Term.
Schedule 1-B
Additional Terms and Conditions for Azurion Release 3 – Technology Maximizer Essential Program (Rev 26.1)
Schedule 1-D
CT Collaboration Live and/or Reacts (Rev 26.1)
| Product Category | Products |
| Computed Tomography | Collaboration Live and/or Reacts |
The following additional terms and conditions apply to CT Collaboration Live and/or Reacts Service (“Software Services”):
Schedule 1-E
Philips OneSpace Insights (Rev 26.1)
| Product Category | Products |
| OneSpace Insights | The Level 0 Basic/ Premium and Level 1 Premium Enterprise Optimization Services |
Schedule 2
Ultrasound Systems Portfolio (UL) (Rev 26.1)
| Product Category | Products |
| Ultrasound Systems (UL) | Cardiovascular Ultrasound (CV UL) |
| General Imaging Ultrasound Systems (GI UL) | |
| Women’s Health Care (WHC UL) | |
| Point of Care (POC UL) |
Schedule 2-A
Collaboration Live or Reacts (Rev 26.1)
| Product Category | Products |
| Ultrasound | Collaboration Live and/or Reacts |
The following schedule will apply if Customer’s purchase includes a license to Collaboration Live and/or the Reacts Platform (“Software Services”).
Schedule 2-B
Lumify (Rev 26.1)
Schedule 2-C
Xtend Coverage (Rev 26.1)
Schedule 2-D
Technology Maximizer Service Package (Rev 26.1)
Schedule 3
Cardiac Informatics Portfolio (CAI) Schedule (Rev 26.1)
| Product Category | Products |
| Cardiology Informatics (CAI) | Hemodynamics (Xper IM, Philips Hemo) |
| IntelliSpace Cardiovascular, Cardiovascular Workspace (ISCV) | |
| IntelliBridge Enterprise Licensed Software (IBE) |
Schedule 4
Hospital Patient Monitoring & Hospital Respiratory Care (HRC) Portfolio (Rev 26.1)<
| Product Category | Products |
| Measurement and Monitors | IntelliVue Patient Monitors and Systems |
| IntelliVue Telemetry System | |
| Fetal Monitors | |
| SureSigns/EarlyVue Vitals Monitors | |
| Clinical Measurements | |
| MR Patient Care Monitors | |
| PerformanceBridge Focal Point | |
| Clinical Informatics | IntelliVue Critical Care and Anesthesia |
| IntelliSpace Perinatal | |
| IntelliBridge Family of Solutions | |
| Sleep Therapy | DreamStation Accessories |
| Hospital Respiratory Care Supplies | Patient Interface (Masks & Cannulas) |
| Circuits | |
| Diagnostic Cardiology Solutions | Stress Testing System (ST80i) |
| Holter Monitoring System (DigiTrak) | |
| Cardiographs (PageWriter) | |
| IntelliSpace ECG |
Schedule 6
Hospital Monitoring & Medical Consumables and Sensors (MCS) Portfolio (Rev 26.1)
| Product Category | Products Consumables and Sensors (non-serialized) | |
| Patient Care | Medical Consumables and Sensors (MCS) | Accessories Third Party Accessories |
| Fetal Measurements | ||
| Gas Measurements | ||
| NIBP Cuffs | ||
| Paper | ||
| SpO2 | ||
| Temperature | ||
| Newborn Solutions | Jaundice | |
| Calming and Soothing Therapy Support | ||
| MR Patient Care (MRPC) | Accessories (disposable and reusable) | |
| ECG | ||
| NIBP Cuffs | ||
| CO2 Supplies | ||
| SPO2 | ||
| Temperature | ||
| Batteries | ||
| Chargers | ||
| Diagnostic Cardiology Solutions | Medical Consumables and Sensors (MCS) | ECG Cables and Lead sets |
| ECG Electrodes | ||
Schedule 7
EI Software and Services Solutions (Rev 26.1)
| Product Category | Products |
| Enterprise Informatics (EI) | Philips Image Management (839060) |
| Philips MyVue | |
| Philips Vue Reporting | |
| Philips Vue Motion | |
| Philips Vue PACS | |
| Philips Vue Explorer (WFM) | |
| Philips Vue Archive |
This Product-specific Schedule is subject to and incorporated into the Conditions of Sale. Without limiting the applicability of Section 13.14 (Product-Specific Terms) therein, the following sections of the Conditions of Sale do not apply to this Schedule 7: 1.4 and 1.6 (Quotation, Order, and Payment), 2 (Lease and Trade-In), and 3.2 and 3.3 (Shipment and Installation).
The following additional terms shall apply to sale of Licensed Software Products (“EI Software and Services Solutions”) under this Schedule:
Schedule 7-A
Annual Maintenance and Support for EI Software and Service Solutions (Rev 26.1)
Schedule 7-B
Additional Terms and Conditions for Clinical and Technical Education Training – EI (Rev 26.1)
Schedule 7-C
HEALTH SUITE IMAGING (“HSI”) (Rev 26.1)
If HSI service is included in the Quotation, the following additional terms shall apply including those set forth in Schedules 7, 7-A and 7-B.
These service terms supplement for HSI (“HSI Supplement”) are incorporated into the EI Schedule by virtue of this reference. In the event terms set forth herein expressly conflict with terms set forth in the EI Schedule, the terms set forth herein shall govern and control in such instance.
HSI provides Hardware and/ or Software running off-premise remotely / on cloud (“Cloud”), i) in lieu of those otherwise provided on-premises or maintain Hardware and/or Software on-premises under its, or ii) add data archival on Cloud for redundancy as detailed in the Quotation. All is as detailed under the following additional terms.
Total number of minutes in a Monthly Period – Minutes of Unscheduled Downtime X 100%
Total number of minutes in a Monthly Period
For purposes of the uptime service level obligation, a 31-day month has 44,640 minutes, a 30-day month has 43,200 minutes, a 29-day month has 41,760 and a 28-day month has 40,320 minutes.
| UPTIME PERFORMANCE | DISCOUNT |
| 99.99% < x | None |
| 99.5% < x < 99.99% | 5% |
| 99.0% < x < 99.5% | 10% |
| x < 99.0% | 15% |
Schedule 7-D
Philips HealthSuite Imaging (“HSI”) Data Protection Service (Rev 26.1)
If HSI Data Protection Service is included in the Quotation, the following additional terms shall apply in addition to those set forth in Schedules 7, 7-A, and 7-B.
Schedule 8
MRI Coil and Disease Management Solutions Portfolio (Rev 26.1)
| Product Category | Products |
| Magnetic Resonance Imaging (MRI) Coils | Capital Coils |
| Consumables | Consumables Coils |
| Disease Management Solutions | UroNav and DynaCAD |
STANDARD PRODUCT WARRANTY PERIODS
MRI Coils - Three years, parts and factory repair labor
Disease Management Solutions Products - One (1) year, parts and factory repair labor
Sentinelle coils – One year, parts and factory repair labor
Parts and Accessories – 90 days, replacement Supplies
Consumable Items and repaired product – 30 days, replacement
Schedule 9
Non Diagnostic Enterprise Operational Informatics (EOI) Software Solutions Schedule (Rev 26.1)
| Product Category | Products |
| Non Diagnostic Enterprise Operational Informatics (EOI) Software Solutions | PerformanceBridge Software Solutions |
This Product-specific Schedule is subject to and incorporated into the Conditions of Sale. Without limiting the applicability of Section 13.14 (Product-Specific Terms) therein, the following sections of the Conditions of Sale do not apply to this Schedule 9: 1.4 and 1.6 (Quotation, Order, and Payment), 2 (Lease and Trade-In), and 3.2 and 3.3 (Shipment and Installation).
Schedule 9-A
Annual Maintenance and Support for the EOI Software Solutions (Rev 26.1)
**Unless specifically included elsewhere in this Agreement, software versions and updates do not include applications that were not purchased with the EOI Software Solutions, including any third party software, such as virus protection software, third party custom interface software, operating system software for client device or server hardware.
Schedule 10
Clinical Insights Manager (Rev 26.1)
Schedule 10-A
Clinical Insights Manager (Rev 26.1)
| Availability | This is the guaranteed access to the Software on the Production Environment, excluding the Scheduled Downtime. |
| On Premise Software (CIM Collector) | The software component of the CIM Collector provided by Philips that will be installed on Customer-provided Virtual Environment. |
| Customer Provided Infrastructure | The hardware and the Virtual Environment provided by Customer on which the Software runs. |
| Philips Production Environment | The cloud-based environment that is maintained by Philips to store and access data built and hosted on Philips' Health Suite Digital Platform ("HSDP"). Excludes any test or acceptance environment. |
| Maintenance Window | The agreed periods during which Scheduled Downtime takes place to perform maintenance for:
|
| Priority | The relative evaluation of a Ticket's priority with respect to other Tickets. |
| Modification | A supplement, change or deletion in the Subscription Service. |
| Response Time | The time that lapses between the moment a Ticket is submitted and the moment Philips shares the first feedback on the Ticket status (Assigns Priority) with Customer. |
| Scheduled Downtime | The time that the Subscription Service is unavailable due to scheduled maintenance, as further detailed under section 3.2. |
| Software | Collectively or individually, the On Premise Software, or software components deployed in the Philips Production Environment, delivered by Philips to Customer, as further specified herein. |
| Support Desk | The point of contact with Philips for providing support on the Subscription Service to Customer (Customer Service Center) |
| Support System | The information system in which Customer support requests are registered. |
| Ticket | A support request submitted by Customer to the Support Desk in the Philips Support System, including issues, requests, questions or other notifications regarding the Subscription Service. |
| Working Day/Hours | The Philips Customer Service Center is available weekdays 8AM-5PM local time at 800-722-9377. |
| Workaround | A method indicated by Philips to avoid the consequences of an issue as far as possible, without the need for a new update to Subscription Service, which enables Customers to use the Subscription Service uninterrupted as far as possible. |
| Section | Service |
| 1 | Installation/Configuration and Onboarding |
| 2 | Technical Support |
| 3 | Subscription Service updates (Including Maintenance Window) |
| 4 | Privacy |
Schedule 11-A
CYBERSECURITY ASSESSMENT TERMS AND CONDITIONS (Rev 25.2)
Schedule 11-B
ANTIVIRUS MANAGEMENT SERVICES TERMS AND CONDITIONS (Rev 25.2)
Schedule 12
Interoperability Solutions (Rev 25.2)
| Product Category | Products |
| Data Management & Interoperability Solutions | HealthSuite Interoperability Solution |
This Product-specific Schedule is subject to and incorporated into the Conditions of Sale. Without limiting the applicability of Section 19 (Product-Specific Terms) therein, the following sections of the Conditions of Sale do not apply to this Schedule 12: 2.4 -2.5 (Quotation, Order, and Payment), 3 (Philips Security Interest until Full Payment), 5 (Lease and Trade-In), 6 (Shipment and Delivery Date), 7.1, 7.3, 7.4 (Installation), and 8 (Product Damages and Returns).
Schedule 12-A
Interoperability Solutions Maintenance and Support Terms and Conditions (Rev 25.2)
The Technical Support Services provided by Philips shall not extend to the following items (nor consequences thereof):
If Customer has purchased Professional Services under this Schedule, then subject to Customer meeting its payment obligations hereunder, Philips will provide Professional Services in accordance with each applicable Quotation, this attachment and the Schedule. The Professional Services may include advice and recommendations. However, Customer (and not Philips) shall at all times be responsible for any decisions based upon such advice or recommendations. Customer acknowledges and agrees that Customer is solely responsible for independently verifying the results of any services of a consultative nature and for Customer’s reliance thereon.
Unless otherwise specified in the Quotation(s), Customer is entitled to receive commercially available Upgrades as determined by Philips from time to time during the Term. Unless Customer has purchased Upgrade installation Services, Customer is responsible for installing Upgrades. The following terms and conditions apply to any such Upgrades:
Customer acknowledges and agrees that, as between Customer and Philips or its licensors, Philips owns all worldwide right, title and interest, including all Intellectual Property Rights, in and to:
Schedule 12-B
Service Levels Exhibit
Service Level Summary (Rev 25.2)
| Support Services | Telephone / Remote Support | X |
| Standard Coverage Hours | As defined Above | |
| Extended Coverage Hours (24/7)* | X | |
| Software Services | Updates & Upgrades performed by Customer | X |
| Updates & Upgrades performed by Philips | Can be purchased as Additional Service Days | |
| Response times** Priority 1 & 2 incidents | 30 minutes | |
| Response times** Priority 3, 4, & 5 | 2 hours | |
| Priority 1 Incident Resolution time** –from the time the Incident report is received by Level 3 support | 72 hours | |
| Priority 2 Incident Resolution time **– from the time the Incident report is received by Level 3 support | 120 hours | |
| Priority 3 Resolution time** from the time the problem report is received by support | Commercially reasonable efforts to have issue resolved as soon as reasonably practicable | |
| On-Site/Remote training | Can be purchased as Additional Service Days. | |
| Professional Services | Release notes & Planning | X |
| Other Professional Services | Can be purchased as Additional Service Days. | |
| Customer Site Network Access Selected | (Remote; Coordinated Remote; On-Site (see Section 2.7.2 for details) ) | Coordinated Remote Access |
* Priority 1 and 2 will be addressed 24 x 7 (High priority incidents) and others during standard Coverage Hours
** Response times and Resolution times are only available for Customers who have provided Remote Network Access.
Schedule 13
Radiology Operation Command Center (“Subscription Service”) Schedule (Rev 25.2)
This Product-specific Schedule is subject to and incorporated into the Conditions of Sale (this Product-specific Schedule, together with the Conditions of Sale and the Quotation(s), are referred to as the “Agreement”). Without limiting the applicability of Section 19 (Product-Specific Terms) of the Conditions of Sale, the following sections of the Conditions of Sale do not apply to this Schedule 13: 2.4 -2.5 (Quotation, Order, and Payment), 3 (Philips Security Interest until Full Payment), 5 (Lease and Trade-In), 6.2 (Shipment and Delivery Date), 7.1, 7.3, 7.4 (Installation), and 8 (Product Damages and Returns).
Schedule 14
Additional Terms and Conditions for Technology Maximizer (Rev 25.2)
Clinical Integration & Insights (CI&I) (Rev 26.1)
| Capsule Integration | Capsule Monitor | Capsule Surveillance | |
| Capsule Perpetual Licensed Software Products (requires purchase of annual maintenance and support) |
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| |
| Capsule Subscription Services |
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| |
| Capsule Hardware |
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| Consumables |
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| Services |
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Schedule 17-C
Clinical Integration & Insights (CI&I)
Intended Use Statement(s) (Rev 26.1)
The Philips Medical Device Information Platform (CMDIP) is intended to transfer, store, and convert medical device data for use by medical devices and healthcare information systems, including those that provide clinical monitoring of a patient intended to be relied upon in deciding to take immediate clinical action. The CMDIP does not control or alter the function of any of the medical devices or information systems by or through which data are captured or consumed.
Schedule 17-D
Clinical Integration & Insights (CI&I)
Licenses (Rev 26.1)
| TYPE OF CONNECTIVITY LICENSE | DESCRIPTION |
| Facility | The Facility Connectivity License provides Licensee the right to collect data from an unlimited number of medical devices per bed, for all licensed beds in the Licensee’s Facility as of the effective date of the Facility Connectivity License. This Facility Connectivity License includes non-bed instances such as the emergency, pre-op, OR, and PACU departments, and up to 10% increase of licensed beds above the number indicated in the Order within the same Facility. The Facility Connectivity License is priced per licensed hospital bed, and all licensed beds in the covered facilities must be purchased on a single agreement. If outpatient facilities are included in the scope of integration, their patient locations must be included in the total licensed bed count. The Facility Connectivity License gives Customer the right to use all client side applications. |
| Multi-Connect License | The Multi-Connect License provides Licensee the right to collect data from an unlimited number of medical devices per bed, for the number of beds licensed in an Order. This license provides Licensee the right to connect to medical devices in three different configurations 1. Connectivity hub (e.g., Neuron, Axon, Client) connected to the wall in the patient room. 2. Neuron connected to the medical device (e.g., ventilator, anesthesia gas machine). 3. Network connected medical devices where no connectivity hub is required |
| General Care Connectivity License | The General Care Connectivity License provides Licensee the right to collect data from a vital signs monitor. This monitor can be connected in 3 ways 1. Neuron Chart Xpress Deployment 2. Neuron SmartLinx Vitals Plus deployment 3. Network connected medical devices where no Philips connectivity hub is required (e.g. Philips VS3 wirelessly connected to network). The General Care Connectivity License is licensed per monitor or Neuron, not per bed. |
Clinical Integration & Insights (CI&I)
Support (Rev 26.1)
| INCIDENT DESCRIPTION | RESPONSE PRIORITY |
| Customer reports an Error that causes critical system components to be down interrupting business continuity. *Production Environment only | Critical = 1 |
| Customer reports an Error that prevents users from performing routine daily tasks. *Test or Production Environments | High = 2 |
| Customer reports an Error that affects non-critical components or causes some annoyance but does not affect productivity. *Test or Production Environments | Medium = 3 |
| Customer reports an issue creating minor annoyance or cosmetic defect. *Test or Production Environments | Low = 4 |
| PRIORITY 1 | PRIORITY 2 | PRIORITY 3 | PRIORITY 4 | |
| Initial Response | 1 Hour | 2 Hours | 12 Hours | Next Business Day |
| Status Update Frequency | Daily | Every 2 Days | Monthly | Upon Request |
| Objective for Resolution | 3 Days | 10 Days | Next Release | At Philips’ Discretion |
| POSITION | NAME | CONTACT DETAILS |
| General Support | [email protected] | 800-260-9537 | |
| Sr. Manager, Technical Support | Jody Bregler | [email protected] | 978-482-2312 |
| VP, Professional Services | John Mchutcheon | [email protected] | 978-482-2308 |
Clinical Integration & Insights (CI&I)
Hardware Warranty Terms (Rev 26.1)
The Warranty Terms below apply to Capsule Hardware purchased starting from July 2016. Hardware purchased prior to that time is governed by the warranty in effect at the time of sale.
| Standard Warranty Duration | Extended Warranty Duration, if purchased (within 12 months of order issuance) | |
|---|---|---|
| SmartLinx Axon 110, 410, 810 |
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| Philips Axon 120, 420, 421, 820 |
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| SmartLinx Device Identification Module |
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| Cables (serial and patch) , power cords, power supplies |
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| Mounting solutions (wall mounts or extended poles) |
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| Refurbished SmartLinx Neuron 2 |
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| SmartLinx Neuron 3 |
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| SmartLinx Neuron 3 Connectivity Modules |
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| SmartLinx Dual Battery Dock |
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| SmartLinx Standalone Dual EXTBAT AC Charger |
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| SmartLinx NIBP Module & SunTech Accessories (on Neuron 2) |
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| SmartLinx Alarm Hub |
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| SmartLinx NIBP Monitoring Module & SunTech Accessories (on Neuron 2) |
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| Capsule NIBP Monitoring Module & SunTech Accessories (on Neuron 3) |
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| Masimo SET Pulse Oximeter & Accessories |
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| Nellcor Oximeter & Accessories |
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| Exergen TAT-5000S Temperature Scanner & Accessories |
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| Filac 3000 Temperature Module & Accessories |
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| Masimo ISA Capnography module & Accessories |
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| Barcode Scanner |
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| Roll Stand |
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| Proximity Card Reader Kit (125KHz, 13.56MHz) |
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| Pagers |
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| Paging System |
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| Workstations |
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| Perle Hubs |
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| TERMS | ||
| Warranty Includes | Hardware and accessories purchased directly from Philips. Defects in materials or workmanship under normal use during the warranty period which begins upon delivery of the product. | |
| Warranty Excludes |
Philips does not warrant that third-party-embedded software will be error free. Philips will use commercially reasonable efforts to address such errors. | |
| Extended Warranty Purchase | The Capsule Hardware Extended Warranty may be purchased only at the order issuance or within 12 months after the order issuance. To purchase the Extended Warranty, Licensee must purchase the Extended Warranty for all units of the same type of Capsule hardware that were purchased on the same order. The fees for the Capsule Hardware Extended Warranty will be invoiced upon delivery of the products, or upon order of the Extended Warranty if purchased after the date of product delivery. Extended warranty fees are non-refundable and cannot be transferred to other products. | |
| Remedy | Defective products that are covered by an in force Philips Warranty will be replaced with new, refurbished or equivalent products at Philips’ discretion. Philips does not offer repair services. Replacement products will be the same or newer versions, with the same or greater functionality than the original. Replacement products will be covered by Philips Warranty for the longer of 90 days from delivery or the remainder of the existing warranty period. | |
| RMA Process | To initiate a return for warranty replacement, swap, repair or credit, Licensee must follow the Philips RMA Instructions provided on Philips’ Customer Portal, or available by contacting Philips Customer Service. The Philips RMA Instructions contain additional details and restrictions. | |
| Updated Warranty Terms | All changes to Hardware Warranty are accessible on Philips’ Customer Portal. | |
Schedule 18
Ultrasound Workspace (Tomtec) (Rev 26.1)
| Product Category | Products |
| Enterprise Informatics (EI) | Ultrasound Workspace (Tomtec) |
Schedule 19
Virtual Care Solutions (Rev 26.1)
Schedule 19-A
Solaborate Statement of Work (Rev 26.1)
Restrictions on use and disclosure
The information in this document includes information that is Philips confidential. This document may not be copied or disclosed to third parties by Customer without Philips prior written approval. Upon Philips request, Customer will promptly destroy this document and return it to Philips, as directed by Philips, including any copies.
Until incorporated into a contract, this statement of work is valid for 90 days from the most current revision date.
Document revision history
| Revision | Date | Description | Author |
Signatures
The parties hereto have caused this SOW to be signed and delivered by their duly authorized representatives, as of the SOW effective date.
| Philips | Customer |
| Signed: | Signed: |
| Name: | Name: |
| Title: | Title: |
| Date: | Date: |
| # | Description of the phase | Start Date | End Date | Deliverable |
| 1 | Preparation of hello devices with latest builds | Average 5 days | Hellocare devices prepared with the latest software builds and configurations | |
| 2 | Onboarding | Average 2 days | Customer successfully onboarded onto the Hellocare platform | |
| 3 | Deployment of Hellocare devices | Average 15 minutes per room | Hellocare devices deployed and installed | |
| 4 | Onboarding Nurses and other staff | 1 day onsite, additional virtual days as required | Nurses and other staff members successfully onboarded onto the Hellocare platform | |
| 5 | Training Users | 1 day onsite, additional virtual days as required | Completion of user training sessions for nurses and other staff members on effectively using the Hellocare platform |
Note: mutually agreed upon project plan, including detailed project tasks/responsibilities and durations will be used to determine activation dates.
| Stakeholders | ||||
| ROLE | NAME | TITLE | PHONE | |
| Project Manager | ||||
| Project Owner | ||||
| Senior User | ||||
| (Key) User | ||||
| (Key) User | ||||
General Project Assumptions
| Training | Audience | Estimated Duration | Maximum # of Sessions |
| Hellocare sys admin/technical training | IT support | 2 hr | 1 Session |
| Hellocare user training | Clinical users | 2 hr | 1 Day of sessions, then self-paced online training |
Philips will be onsite to support the phase 1 activation.
In support of the integration efforts, Philips will provide a service lead throughout the duration of each project phase to complete the key project tasks listed below.
Please note, focused ad hoc meetings will be scheduled as needed.
In support of the integration efforts, Philips will provide a technical lead throughout the duration of each project phase to complete the key project tasks listed below.
In support of the integration efforts, Philips will provide an interface lead throughout the duration of each project phase to complete the key project tasks listed below.
Interface Included in project scope are:
| Role | Responsibilities |
| Project Management | • Manages all project scheduling, plan, resources, deliverables, timeline, and critical path milestones. • Acts as the first point of escalation for Hellocare related issues |
| Clinical Transformation Manager | • Guide the development of clinical workflows and procedures • Conduct clinical training of super users to enable end-user training • Assist during the clinical testing effort |
| Technical Consultant | • Load/configure Hellocare platform • Install/configure audio/video devices • Conduct technical training • Provide guidance and support during technical acceptance |
| Interface Analyst | • Conduct the interface mapping and coding effort • Conduct interface training • Provide guidance and support during the interface testing effort |
| Role | Responsibilities |
| Project Management | • Manages assignments, schedules, communication and deliverables for staff assigned to the project • Acts as the primary point of contact for the Philips Project Manager |
| Clinical Lead (s) | • Serve as an overall point of contact and lead • Coordinate clinical activities during the project such as workflow development, and clinical training and testing efforts |
| Technical Lead(s) | • Coordinate technical activities associated with in-room install and workstation configuration to meet the project timeline |
| Interface Lead(s) | • Schedule/Secure testing resources to execute established test plan |
| System Admin/ Support Staff | • Support Hellocare post activation according to available trainings and product documentation • Execute Helpdesk policies and procedures |
Schedule 19-B
OEM Service Level Agreement (Rev 26.1)
| Severity Level | Fault Categories | Response Time | Target Restore Time | Root Cause Removal Time |
| P1 | Critical Fault | 30 Minutes | 4 hours | Work 24/7 until restored or acceptable workaround in place |
| P2 | Major Fault | 1 hour | 24 hours | 5 business days / hotfix |
| P3 | Minor Fault | 1 business day | 5 business days | 10 business days after the target restore time/Next scheduled release or hotfix |
“Response time” shall mean the time interval from the receipt of Customer notification of a problem by OEM within Gitlab, or any other service portal maintained by OEM that Customer has been given access to and confirmation of OEM that it has received the problem and starts with analysis of the problem.
“Target Restore Time” shall mean the time interval from the time when the problem is resolved, which substantially enables resumption of the service that is provided by OEM (problem can also be resolved with a temporary solution or workaround).
“Root Cause Removal Time” shall mean the when the permanent fix for the problem is provided to Customer (root cause of the problem is resolved).
| Priority | Description |
| Critical / Priority 1 | Conditions exist that severely affect the Products or Software. Such problems require immediate corrective action 24 hours a day, 7 days a week. A “Critical Error” is defined as: • An error in the Software or Products in a live environment which results in the Software being rendered inoperable or on which the end-user is unable to perform critical business functions, and for which no temporary workaround is known or available. • An error in the Software or Products causes failure or severe degradation in a live environment that materially and adversely impacts the functionality of the Software or Products and for which no immediate workaround is available. Examples of emergency cases are: • Total outage of the Software • Key functionality not available to over 50% of end users |
| Major / Priority 2 | • Conditions exist that seriously affect Software operation and require attention because of the high possibility to affect end user usage. This may also include a technical request due to some business purposes (product development) or regulatory obligations of Customer. • A “Major fault” is defined as: • Significant loss of Software or Product functionality or the Software has failed to the extent that part of the Software or Products or specific functions are not performing as expected or described in any documentation. • An error causes failure or severe degradation in a live, production environment or during deployment of these environments of one or more functions of the Software that materially and adversely impacts the use by an end user and for which no immediate workaround is available. |
| Minor / Priority 3 | Conditions exist that do not significantly impair the function of the Software or Products and do not significantly affect service to end users, but represent a potential problem or difficulty in utilizing the Software. This may also include a technical request for additional information about system operation, maintenance, administration or service features by Customer. A “Minor fault” is defined as: • An error in the Software and/or Products that is minor in nature; causes minor impact to the end user • An error in the Software or Products that is minor and has no impact to an end user’s business and operations. |
Schedule 20
IntelliSpace ECG Management as a Service (Rev 26.1)
IntelliSpace ECG Solution Management as a Subscription Service provides healthcare clients access to IntelliSpace ECG (ISECG) management software through a cloud environment.
| 1% to 20% increase of the annual ECG Study volume | 20% discount on the fee of the incremental ECG Study volumes |
| 21% and above increase of the annual ECG Study volume | 20% discount on the fee – 1% to 20% of the incremental ECG Study volumes Additional 10% discount on the fee - above 21% of the incremental ECG Study volumes |
Customer may roll up to 10% of the unused ECG Study volume from a contract year to the following year.
For clarity, no refund will be issued for unused ECG Study volume.
Customer will provide:
Schedule 21
Advanced Visualization Workspace (Rev 26.1)
| Product Category | Products |
| Enterprise Informatics (EI) | Philips Advanced Visualization Workspace (aka ISP) |
This Product specific Schedule is subject to and incorporated into the Conditions of Sale. Without limiting the applicability of Section 13.14 (Product Specific Terms) therein, the following sections of the Conditions of Sale do not apply to this Schedule 21: 1.4 and 1.6 (Quotation, Order and Payment), 2 (Lease and Trade-In), and 3.2 and 3.3 (Shipment and Installation).
Schedule 21-A
Annual Maintenance and Support for EI Software and Service Solutions (Rev 26.1)
Schedule 21-B
Additional Terms and Conditions for Clinical and Technical Education Training (Rev 26.1)
Schedule 22
4DMedical Applications Product Specific Schedule (Rev 26.1)
Schedule 22-A
Service Level Agreement
4DMedical Applications
| Customer Provided Infrastructure | The hardware and the virtual environment (VE) provided by Customer on which the Subscription Service runs, including On Premises Software. |
| External Downtime | Unplanned downtime not resulting from Philips or its licensor-controlled software or services (i.e., downtime caused by Customer or 3rd-party issue that is not directly part of Philips and its licensor’s service). |
| Maintenance Window | The agreed periods during which Scheduled Downtime takes place to perform maintenance, Updates and Upgrades for the Subscription Service on the Production Environment. |
| Modification | A supplement, change or deletion in the Subscription Service. |
| On Premises Software | The software component of the Subscription Service provided by 4DMedical on behalf of Philips that will be installed on Customer-Provided Infrastructure. |
| Priority | The relative evaluation of a Ticket's priority with respect to other Tickets. |
| Production Environment | The cloud‑based environment or on-premises environment, where all processing and storage for the Subscription Service takes place. This environment is dedicated to production use and does not include any test or acceptance systems. |
| Response Time | The time period between when a Ticket is submitted and when Philips, or its licensor, shares the first feedback on the Ticket’s status and assigns Priority with Customer. |
| Scheduled Downtime | The time that the Subscription Service is unavailable due to scheduled maintenance. |
| Service Outage | Any event that renders the Subscription Service unavailable to Customer other than (i) Scheduled Downtime or (ii) External Downtime. |
| Subscription Service Guide | The instructions for use and/or technical documents regarding the Subscription Service. |
| Support Desk | The point of contact with Philips or it’s licensor 4DMedical, for providing support on the Subscription Service to Customer (Customer Service Center) |
| Support System | The information system in which Customer support requests are registered. |
| Ticket | A support request submitted by Customer to the Support Desk in the Support System, including issues, requests, questions or other notifications regarding the Subscription Service. |
| Working Day/Hours | The Support Desk is available 8 AM to 6 PM CST; Monday through Friday, excluding holidays. |
| Workaround | A method indicated by Philips, or it’s licensor, to avoid the consequences of an issue as far as possible, without the need for a new update to the Subscription Service, which enables Customers to use the Subscription Service uninterrupted as much as possible. |
Service Overview (Table 1)
| Section | Service |
| 1 | Installation/Configuration and Onboarding |
| 2 | Technical Support |
| 3 | Support Response times |
| 4 | Error Workaround and Resolution |
| 5 | Subscription Service Updates (during Maintenance Window) |
Support Response Times (Table 2)
| Classification | Response | |
| Severity 1* | Within 2 business hours | |
| Severity 2* | Within 6 business hours | |
| Severity 3 | Within 5 business days | |
| Severity Levels Classification Description | ||
| Severity 1: | “Critical Business Impact” The impact of the deficiency reported in the Support Request is such that a User is unable either to use the Application or reasonably continue work using the Application. | |
| Severity 2: | “Significant Business Impact” Important features of an application are not working properly, and there are no acceptable alternative solutions. While other areas of the Application may not be impacted, the deficiency reported in the Support Request has created a significant, negative impact on a User’s productivity or service level. | |
| Severity 3: | “Some Business Impact/Minimal User Impact” Important features of an application are unavailable, but an alternative solution is available, or non-essential features of the Application are unavailable with no alternative solution. The User impact, regardless of product usage, is minimal loss of operational functionality or implementation resources. | |
Workaround Classification (Table 3)
| Classification | Workaround |
| Severity 1 | Within 24 hours of the Ticket creation |
| Severity 2 | Within 48 hours of the Ticket creation |
| Severity 3 | Not applicable |
Schedule 23
IntelliSpace Cardiovascular Workspace (Rev 26.1)
| Product Category | Products |
| Enterprise Informatics (EI) | IntelliSpace Cardiovascular Workspace |
Schedule 23-A
IntelliSpace Cardiovascular Service Level Agreement
This is the Service Level Agreement describing the Maintenance, Technical Support, and other Services provided for Philips’ IntelliSpace Cardiovascular solution (the “Subscription Service”). This Agreement is subject to the Subscription Service terms and conditions agreed between the Customer and Philips or the Philips authorized reseller making Subscription Service available to Customer (the “Agreement”).
| Topic | Entitlement Description | |
| Self-Help Resources | User Manuals | |
| Support Channels | Customer Service Portal (ServiceNow) and Customer Support number | |
| 24x7 Telephone and Remote Support | Coverage services are available 24 hours per day, 7 days per week, including Philips recognized holidays. | |
| Clinical Telephone and Remote Support. | Clinical support is available Monday through Friday between 8:00 AM – 5:00 PM local time, excluding Philips-recognized holidays | |
| Availability | 99.9% Subscription Service Uptime (excludes Scheduled and External Downtime) | |
| Support Initial Response Time | Priority 1 | 1 hour |
| Priority 2 | 4 Hour | |
| Priority 3 | 8 Hours | |
| Priority 4 | 5 Days | |
| Maintenance | Upgrades and Updates (Frequency & Timing set by Philips) | |
| Disaster recovery | Disaster Recovery Protocol and Data Backup | |
| Reports | When a Priority 1 incident occurs (system down) a root cause analysis will be performed and made available after max. 15 working days | |
Subscription Service Software Release Classification (Figure 1)
| Type of release | Number | Deployment | Description |
|---|---|---|---|
| Major release (X) | 1 | By request | An increment to the “Major” number (X) is required due to a release with regulatory significant new features or functions, platform or functions changes, and/or new or changed technology. It can also include changes to the intended use. |
| Minor release (Y) | 1.YY | By request | An increment to the “Minor” number (Y) is required due to release with fixes, enhancements, new features or functions that do not impact software safety or operating efficiency. |
| Software level release (Z) | 1.YY.ZZZZ | By request | An increment to the “Level” number (Z) is required for a release with non-regulatory significant features or function changes to bring the software back to the original specification / intended performance; and that does not impact safety or effectiveness; and where the changed software is fully compatible with the current (unchanged) software. |
| Service Pack (a) | 1.YY.ZZZZ.aa | As necessary | An increment to the “Service Pack” number (a) is required due to corrective maintenance for Customer specific request(s) that need an immediate fix. Service Pack is for a specific Customer or a limited set of Customers. Unlike typical level updates, a service pack is urgently developed and released as soon as practicable to limit the effects of the software issue. It is often released between incremental level updates. |
For purposes of the uptime performance warranty, a 31-day month has 44,640 minutes; a 30-day month has 43,200 minutes; a 29-day month has 41,760 minutes; and a 28-day month has 40,320 minutes.
Monthly Availability Targets (Figure 2)
| Availability Measurement | Monthly Fee Credit |
| Less than 99.9% but equal to or greater than 99.0% | 5% |
| Less than 99.0% but equal to or greater than 98.0% | 10% |
| Less than 98.0% | 15% |
The Equipment and Disposable Products listed in this Agreement is offered by Philips ("Philips") only under the terms and conditions described below (the “Standard Terms and Conditions”).
The purchase price stated in this Agreement does not include applicable sales, excise, use, other taxes, or government surcharges in effect or later levied. Customer shall provide Philips with appropriate exemption certificate reasonably in advance of the date the Equipment and/or Disposable Product is available for delivery, otherwise, Philips shall invoice Customer for those taxes, as well as any government surcharges, and Customer shall pay those taxes in accordance with the terms of the invoice. Government surcharges are non-exempt under law. Customer is defined as a legal entity its affiliates and or subsidiaries who purchase Equipment and/or Disposable Products and take title of the purchased Equipment and/or Disposable Products from Philips.
Philips may file a financing statement for such security interest and Customer shall sign any financing statements or other documents necessary to perfect Philips’ security interests in the Equipment and/or Disposable Products.
Prior approval by Philips is required to return Disposable Products for credit or exchange. Such approval may be requested by contacting Philips Customer Service as specified on the attached Contact Information sheet. Disposable Products may be returned due to: (i) damage prior to receipt by Customer or failure to conform to the specifications, in which case, Philips shall credit Customer for the amount of the return shipping fees; (ii) incorrect Disposable Product(s) received, in which case Philips will issue a call tag and provide a return shipping label for Disposable Product; or (iii) incorrect Disposable Product(s) ordered, in which case Customer must report such incorrect order to Philips within fifteen (15) days of Customer’s receipt of Disposable Product(s). In the instance of any return, Philips may require a new or revised purchase order for the replacement order. Except in the instance of (i) above, Disposable Products will only be considered for exchange or credit if the item is in its original packaging, with no visible marks or damage, and the sterile packaging remains uncompromised. No credit or exchange will be issued for items returned in unsaleable condition. Unless otherwise explicitly agreed to in this Agreement or an Exhibit, Philips does not accept returns of excess inventory, for stock rotation, or other exchange programs. Upon approval of the request to return, which approval will not be unreasonably withheld, Philips will issue a Return Material Authorization (RMA) number. The RMA number must be included on all returned Disposable Product shipping cartons (do not write this number directly on the product package).
IN NO EVENT SHALL PHILIPS OR ITS AFFILIATES BE LIABLE FOR ANY INDIRECT, PUNITIVE, INCIDENTAL, CONSEQUENTIAL, EXEMPLARY OR SPECIAL DAMAGES, INCLUDING WITHOUT LIMITATION, LOST REVENUES OR PROFITS, BUSINESS INTERRUPTION, LOSS OF DATA, OR THE COST OF SUBSTITUTE EQUIPMENT AND/OR DISPOSABLE PRODUCTS OR SERVICES WHETHER ARISING FROM BREACH OF CONTRACT, BREACH OF WARRANTY, NEGLIGENCE, INDEMNITY, STRICT LIABILITY OR OTHER TORT.
Each party shall maintain as confidential any information furnished or disclosed to one party by the other party, whether disclosed in writing or disclosed orally, relating to the business of the disclosing party, its customers, employees, and/or its patients, and the Agreement and its terms, including the pricing terms under which Customer has agreed to purchase the Equipment and/or Disposable Products. Each party shall use the same degree of care to protect the confidentiality of the disclosed information as that party uses to protect the confidentiality of its own information, but in no event less than a reasonable amount of care. Each party shall disclose such confidential information only to its employees having a need to know such information to perform the transactions contemplated by the Agreement. The disclosing party maintains exclusive ownership of the confidential information which it discloses to the receiving party, and a receiving party shall be responsible for the breach of these confidentiality terms by any of its representatives or other person to whom it may disclose the confidential information. The obligation to maintain the confidentiality of such information shall not extend to information that (a) is or becomes generally available to the public without violation of these Standard Terms and Conditions or any other obligation of confidentiality or (b) is lawfully obtained by the receiving Party from a third party without any breach of confidentiality or violation of law. Notwithstanding the foregoing, in the event that the receiving party is required by law to disclose any confidential information to a court, government department/ agency or regulatory body, the receiving party may so disclose, provided that it shall, to the extent permitted by applicable law, first inform the disclosing party of the request or requirement for disclosure to allow an opportunity for the disclosing party to apply for an order to prohibit or restrict such disclosure. Moreover, nothing set forth herein shall prohibit Customer from disclosing confidential information required by state or federal open records laws, to the extent disclosed in compliance with the rules and procedures applicable thereto, including notifying Philips and providing Philips an opportunity to argue certain information may be exempt as a trade secret, if applicable thereunder.
As of the date of the sale of this Equipment and/or Disposable Products, Philips represents and warrants that Philips, its employees and subcontractors, are not debarred, excluded, suspended or otherwise ineligible to participate in a federal or state health care program, nor have they been convicted of any health care related crime for the Equipment and/or Disposable Products and services provided under these Standard Terms and Conditions (an "Excluded Provider"). Philips shall promptly notify Customer if it becomes aware that Philips or any of its employees or subcontractors providing services hereunder have become an Excluded Provider under a federal or state healthcare program, whereupon Customer shall provide Philips with a reasonable opportunity to discuss and attempt to resolve in good faith with Customer any Customer related concerns in relation thereto, and/or will give Philips a reasonable opportunity to dispute its, or its employee’s or subcontractor’s, designation as an Excluded Provider. In the event that the Parties are unable to resolve any such Customer concerns of the applicable party’s designation as an Excluded Provider, then Customer may terminate this order by express written notice for Equipment and/or Disposable Products and services not yet shipped or rendered prior to a date of exclusion.
Philips and Customer shall comply with the Omnibus Reconciliation Act of 1980 (P.L. 96-499) and its implementing regulations (42 CFR, Part 420). Philips agrees that until the expiration of four (4) years after furnishing services or Equipment and/or Disposable Products pursuant to these Standard Terms and Conditions, Philips shall make available, upon written request of the Secretary of the Department of Health and Human Services, or upon request of the Comptroller General, or any of their duly authorized representatives, these Standard Terms and Conditions and the books, documents and records of Philips that are necessary to verify the nature and extent of the costs charged to Customer hereunder. Philips further agrees that if Philips carries out any of the duties of these Standard Terms and Conditions through a subcontract with a value or cost of ten-thousand U.S. dollars ($10,000.00) or more over a twelve (12) month period, with a related organization, such subcontract shall contain a clause to the effect that until the expiration of four (4) years after the furnishing of such services pursuant to such subcontract, the related organization shall make available, upon written request to the Secretary, or upon request to the Comptroller General, or any of their duly authorized representatives the subcontract, and books and documents and records of such organization that are necessary to verify the nature and extent of such costs. This paragraph relating to the retention and production of documents is included because of possible application of Section 1861(v) (1) (1) of the Social Security Act (42 U.S.C. 1395x (v) (1) (I) (1989)), as amended from to time to these Standard Terms and Conditions. If Section 1861(v) (1) (1) should be found to be inapplicable, then this paragraph shall be deemed inoperative and without force and effect.
Customer represents and warrants that the Equipment and Disposable Products are being acquired solely for the Customer’s own use at the Customer facility(ies) listed herein. Customer shall not resell the Equipment and/or Disposable Products.
Company agrees not to analyze for composition, software, internal elements, structure or reverse engineer or transfer to any third party for analysis, reverse engineering, or any other purpose, any Disposable Products and or Equipment without the express prior written consent of Philips.
If equipment is rented under this Agreement, Customer agrees to delete all data collected on the equipment (with Philips’ reasonable instructions) including specifically any and all data constituting Protected Health Information as that term is defined in 45 CFR 164.502(d) prior to returning the Equipment to Philips at the expiration of any rental term under this Agreement.
Customer agrees that Philips may periodically remotely connect to Philips equipment and collect and use information from the system log file for Philips’ own business purposes (including, but not limited to, for data analytics activities, to facilitate and advise on continued and sustained use of Philips’ or its affiliates’ products and services, for research, product and service development and improvement (including the development of new offerings), substantiation of marketing claims and for benchmarking purposes). The system log file does not contain any protected health information (within the meaning of the HIPAA Privacy Rule) or any information that is capable of identifying an individual.