PROJECT OUTPUT Sample Clauses

PROJECT OUTPUT. Output 8. The output of this Agreement will be the redesign of clinical trials systems through: (a) establishing new and enhanced central coordination units or equivalent that will: i. play a key ‘gateway’ role for sponsors, investigators, referrers and participants accessing and navigating trials; ii. reduce the administrative load on trial sites through the provision and/or facilitation of key trial operational functions (e.g., feasibility assessment, ethics clearance, site authorisation, trial governance, insurance and contract management); iii. act as central points for communication, training and education; iv. support patient recruitment and the conduct of clinical trials; v. support the clinical trial workforce through building capacity and capability, ensuring quality control and pooling resources to provide career pathways and professional development; and vi. work across jurisdictions towards a consistent and cohesive national approach to the conduct of clinical trials, including implementing agreed standards; (b) implementing new and enhanced clinical trial data collection and reporting to inform systems improvement with interoperability and data flow capability, and contribute to better sector knowledge, recruitment and overall sector performance including through: i. implementation and continued expansion of clinical trials metrics collection including those agreed under the Framework for National Aggregate Statistics (NAS); and ii. ongoing submission of agreed metrics to the national data collection in accordance with the Framework for NAS; (c) establishing and maintaining new networks and partnerships within and between jurisdictions, clinical trial networks, communities of practice (eg. oncology, working with ATSI groups) and registries; and (d) embedding research and clinical trials processes into core hospital governance arrangements. 9. The States are collectively responsible for delivering these outputs, which reflect the revitalised clinical trials agenda endorsed by Health Ministers in March 2017. In support of these outputs, each jurisdiction is responsible for delivering the projects agreed in its bilateral Schedule to this Agreement.

PROJECT OUTPUT. Outputs To recover water and maintain water pressure within the Basin, the outputs of this Agreement will be the: replacement of old bores legally operating in an uncontrolled state with controlled bores and efficient, controlled watering systems; and restoration of critical infrastructure assets. Part 3 — roles and responsibilities of each party Role of the Commonwealth In addition to the roles and responsibilities set out in Schedule A, the Commonwealth will be responsible for: monitoring and assessing achievement against milestones in the delivery of the Interim Great Artesian Basin Infrastructure Investment Program under this Agreement to ensure that outputs are delivered within the agreed timeframe; and providing a consequent financial contribution to Queensland to support the implementation of this Agreement. Role of Queensland In addition to the roles and responsibilities set out in Schedule A, Queensland will be responsible for: providing a financial contribution to support the implementation of this Agreement; all aspects of implementation of Project Outputs set out in this Agreement; and reporting on the delivery of outputs as set out in Part 4 – Project Milestones, Reporting and Payments. Shared roles The Commonwealth and Queensland will: be jointly responsible for developing and agreeing to the project list (Schedule B), in accordance with Part 4 – Project Milestones, Reporting and Payments, and Schedule A to this Agreement, concurrently with or as soon as possible following the signing of this Agreement, a list of projects to be completed by 30 April 2020; and meet the requirements of Schedule E, Clause 26 of the IGA FFR, by ensuring that prior agreement is reached on the nature and content of any events, announcements, promotional material or publicity relating to activities under this Agreement, and that the roles of both Parties will be acknowledged and recognised appropriately.

PROJECT OUTPUT. Output 8. The output of this Agreement will be increased access to compression garments for eligible patients in Queensland by: (a) contributing to the Lymphoedema Compression Garment Scheme in Queensland; and/or (b) contributing to activities that promote increased access to allied health professionals appropriately trained in the prescription of compression garments for lymphoedema; and/or (c) contributing to activities that increase access to allied health professionals to enable the timely assessment of patients requiring compression garments.

PROJECT OUTPUT. Output 7. The output of this Agreement will be the delivery of projects that reduce the regulatory burden on small business. Project Agreement for Small Business Regulatory Reform PART 3 — ROLES AND RESPONSIBILITIES OF EACH PARTY 8. The Commonwealth will be responsible for: (a) assessing and agreeing the State-nominated projects to be funded; (b) monitoring and assessing achievement against milestones in the delivery of regulatory reform for small business under this Agreement to ensure that outputs are delivered within the agreed timeframe; and (c) providing a consequent financial contribution to the States to support implementation of this Agreement. 9. The States will be responsible for: (a) submitting project proposals and supporting evidence; (b) all aspects of delivering on the outputs set out in this Agreement; and (c) reporting on the delivery of the output as set out in Part 4 – Project Milestones, Reporting and Payments.

PROJECT OUTPUT. Output 8. The output of this Agreement will be effective control of Yellow Crazy Ant infestations in and adjacent to the Wet Tropics of Queensland World Heritage Area.

PROJECT OUTPUT. Publications: Any project-related articles, papers, or presentations that are authored or prepared by the Project Team and published or distributed (at a conference or otherwise). List author name; title; publication or conference; volume, issue, and pages (if applicable); and year of publication. The Prime Recipient is required to send a copy of each publication to the program support designated by the EERE Program Director. Scientific/technical conference papers/proceedings must also be reported in accordance with Section II.B of “EERE Reporting Instructions.”

PROJECT OUTPUT. Output The output of this Agreement will be increased access to compression garments for eligible patients in Western Australia by: contributing to the establishment of a Lymphoedema Compression Garment Scheme in Western Australia; and/or contributing to activities that promote increased access to allied health professionals appropriately trained in the prescription of compression garments for lymphoedema; and/or contributing to activities that increase access to allied health professionals to enable the timely assessment of patients requiring compression garments. Part 3 — roles and responsibilities of each party Role of the Commonwealth The Commonwealth will be responsible for: monitoring and assessing achievement against milestones in the delivery of the Lymphoedema Compression Garment Scheme under this Agreement to ensure that outputs are delivered within the agreed timeframe; and providing a consequent financial contribution to Western Australia to support the implementation of this Agreement. Role of Western Australia Western Australia will be responsible for: all aspects of delivering on the project outputs set out in this Agreement; and reporting on the delivery of outputs as set out in Part 4 – Project Milestones, Reporting and Payments.

PROJECT OUTPUT. Output The output of this Agreement will be increased access to compression garments for eligible patients in Victoria by: contributing to the Lymphoedema Compression Garment Scheme in Victoria; and/or contributing to activities that promote increased access to allied health professionals appropriately trained in the prescription of compression garments for lymphoedema; and/or contributing to activities that increase access to allied health professionals to enable the timely assessment of patients requiring compression garments. Part 3 — roles and responsibilities of each party Role of the Commonwealth The Commonwealth will be responsible for: monitoring and assessing achievement against milestones in the delivery of the Lymphoedema Compression Garment Scheme under this Agreement to ensure that outputs are delivered within the agreed timeframe; and providing a consequent financial contribution to Victoria to support the implementation of this Agreement. Role of Victoria Victoria will be responsible for: all aspects of delivering on the project outputs set out in this Agreement; and reporting on the delivery of outputs as set out in Part 4 – Project Milestones, Reporting and Payments.

PROJECT OUTPUT. Output 8. The output of this Agreement will be the commencement of the establishment of the ONRSR in Adelaide by the National Rail Safety Regulator (NRSR) Project Office.

PROJECT OUTPUT. Output 8. The output(s) of this Agreement will be improved detection, monitoring and management of the infectious disease ARF and the resultant condition RHD through: (a) implementation of a dedicated state wide patient register and recall system for ARF and RHD; (b) implementation of strategies to facilitate improved clinical care including improved delivery of and adherence to secondary prophylaxis antibiotics; (c) promotion of education and training for health care providers, individuals, families and communities; and (d) collection and provision of data for national monitoring and reporting of ARF and RHD and measuring program effectiveness in the detection and management of ARF and RHD.