Obligations and Responsibilities Sample Clauses

Obligations and Responsibilities. 3.1 General obligations and role of the beneficiaries (including the coordinator). The beneficiaries: (a) are jointly responsible for carrying out the activities attributed to them, and shall conduct the work in accordance with the work programme and schedule set forth in the Grant Agreement and approved application, working to the best of their abilities to achieve the defined results and taking full responsibility for their work in accordance with accepted professional principles; (b) undertake to comply with all the provisions of the Grant Agreement and its annexes, with all the provisions of this Agreement, as well as with EU and national legislation; (c) are jointly responsible for complying with any legal obligations incumbent on them jointly or individually; (d) shall provide staff, facilities, equipment and material to the extent needed for executing the activities as specified in the work programme; (e) shall be responsible for the sound financial management and cost efficiency of the funds allocated to the project. 3.2 Specific obligations and role of the coordinator. The coordinator undertakes to: (a) be responsible for the overall coordination, management and implementation of the project in accordance with the Grant Agreement; (b) be the intermediary for all communication between the beneficiaries and the Executive Agency, and inform the beneficiaries of any relevant communication exchanged with the Executive Agency; (c) inform the beneficiaries of any changes connected to the project or to the Grant Agreement, or of any event likely to substantially affect the implementation of the action; (d) as the sole recipient of payments on behalf of all beneficiaries, transfer funds to the beneficiaries without unjustified delay and in accordance with the dispositions for payments laid down in Article 5 of this Agreement; (e) manage and verify the appropriate spending of the funds in accordance with the dispositions of the Grant Agreement and this Agreement; (f) comply with all reporting requirements vis-à-vis the Executive Agency, as per the dispositions of Article I.4

Obligations and Responsibilities. 3.1 General obligations and role of the beneficiaries (including the coordinator). The beneficiaries shall: (a) be jointly and severally responsible for carrying out the action in accordance with the terms and conditions of the Grant Agreement and approved application, working to the best of their abilities to achieve the defined results and taking full responsibility for their work in accordance with accepted professional principles; (b) be responsible for complying with any legal obligations incumbent on them jointly or individually; (c) make appropriate internal arrangements for the proper implementation of the action, consistent with the provisions of the Grant Agreement and its Annexes; provisions of this Agreement, as well as with E U and national legislation; (d) be responsible for the sound financial management and cost efficiency of the funds allocated to the project. 3.2 Specific obligations and role of the coordinator. The coordinator shall: (a) be responsible for the overall coordination, management and implementation of the project in accordance with the Grant Agreement; (b) be the intermediary for all communication between the beneficiaries and the Executive Agency, and inform the beneficiaries of any relevant communication exchanged with the Executive Agency; except where provided otherwise in the Agreement: (c) immediately provide the Executive Agency with the information related to any change in the name, address, legal representative as well as in the legal, financial, technical, organisational or ownership situation of any o f the beneficiaries or of its affiliated entities or to any event likely to affect or delay the implementation of the action, of which the coordinator is aware (d) bear responsibility for supplying all documents and information to the Executive Agency which may be required under the Grant Agreement, except where provided otherwise in the Grant Agreement; where information is required from the other beneficiaries, the coordinator shall bear responsibility for obtaining and verifying this information before passing it on to the Executive Agency; (e) inform the beneficiaries of any changes connected to the project or to the Grant Agreement, or of any event likely to substantially affect the implementation of the action; (f) as the sole recipient of payments on behalf of all beneficiaries, transfer funds to the beneficiaries in accordance with the dispositions for payments laid down in the Grant Agreement; subject to imp...

Obligations and Responsibilities. (1) You agree to comply with and abide by policies listed in the Student Handbook to include the Honor Code, the Social Code, and any other College policies. (2) You agree to pay all charges as due to the College.

Obligations and Responsibilities. The Complainant The Respondent

Obligations and Responsibilities. The Institution is responsible for ensuring that the Principal Investigator: (1) thoroughly familiarises himself or herself with the appropriate use of the Investigational Product(s), as described in the Protocol, Investigator’s Brochure, information relating to the Investigational Product and any other information sources provided by the Sponsor; (2) ensures written approval has been obtained to conduct the Study from the Responsible HREC and the Institution prior to Study initiation. Written documentation of approval by the Responsible HREC and the Institution must be provided to the Sponsor; (3) conducts the Study according to the Protocol without changes except as provided in clause 2.2, or as agreed to in writing by the Sponsor and the Institution and approved in accordance with clause 3.3(5) (4) completes (and obtains completion from relevant Personnel) and returns to the Sponsor a statement of financial disclosure (an example that meets this requirement is Food and Drug Administration Form 3455 ‘Disclosure: Financial Interests and Arrangements of Clinical Investigators) before the commencement of the Study and as otherwise required and consents to the disclosure of the completed form to overseas regulatory agencies, if required; (5) ensures that any amendments to the Protocol are approved by the Responsible HREC and Sponsor prior to implementation of the amendment; (6) ensures that the Sponsor’s prior written consent is obtained to any advertisement in respect of the Study; (7) provides the Sponsor with evidence of the Principal Investigator’s qualifications through a current curriculum vitae and/or other relevant documentation and a list of appropriately qualified persons to whom they have delegated significant Study-related duties, if required; (8) uses his or her best endeavours to recruit the target number of Study Subjects, within the recruitment period, specified in Schedule 1, provided that if the overall target number of Study Subjects for the Study is reached, the Sponsor may direct the Institution to cease recruitment; (9) is available when a clinical research representative of the Sponsor visits the Study Site, as mutually agreed prior to the visit, and is contactable by telephone or electronic mail as frequently as is reasonably required; (10) notifies the Sponsor, the Institution and the Responsible HREC of any Adverse Events (including Serious Adverse Events) that occur during the course of the Study in accordance with the Protocol, an...

Obligations and Responsibilities. (1) If the Principal Investigator leaves the Institution or otherwise ceases to be available then: (a) the Institution must consult with the Sponsor and use reasonable endeavours to nominate as soon as practicable a replacement reasonably acceptable to both Parties; and (b) the Sponsor may require recruitment into the Study by the Institution to cease, or move the Study to a different study site. (2) If the Principal Investigator fails to carry out those obligations specified in clauses 3.3(2), (3), (5), (8), (10), (11), (13) ,(15), then the Institution must itself perform those obligations and rectify and make good any breach. The Institution will ensure that any Personnel who assist in the conduct of the Study are informed of and agree to abide by all terms of this Agreement relevant to the activities they perform. (3) The Institution warrants that to the best of its knowledge, it, its affiliates and any person involved in the conduct of the Study, including the Principal Investigator, are properly registered with appropriate professional registration bodies, have not been disqualified from practice or disbarred or banned from conducting clinical trials by any Regulatory Authority for debarment. Furthermore, the Institution shall notify the Sponsor as soon as practical after it becomes aware of any such disqualification, disbarment or ban. (4) The Institution will not engage in any conduct on the Sponsor’s behalf which is in violation of, or potentially in violation of, any applicable local or foreign laws or regulations. (5) The Institution must have adequate security measures to ensure the safety and integrity of the Investigational Product, Essential Documents and Study records and reports, Equipment and any Study related materials held or located at the Study Site. (6) Subject to clause 9, the Institution will allow regular monitoring visits in accordance with the GCP Guideline, access for the purposes of audit and as required by Regulatory Authorities or as specified in the Protocol and permit access to the Essential Documents (including original records), Study records, reports, other Study related materials and its Personnel as soon as is reasonably possible upon request by the Sponsor, Regulatory Authority, Responsible HREC or any third party designated by the Sponsor. Any such access to take place at times mutually agreed during business hours and subject to such reasonable conditions relating to occupational health and safety, security, and con...

Obligations and Responsibilities. The Roommates agree to the following set of obligations and responsibilities: A. Washing Dishes: Each Roommate is responsible for the timely cleaning, drying and putting away those dishes which he or she, or his or her guests, use.

Obligations and Responsibilities. The following obligations shall be the responsibility of QuantumShift, which obligations, unless otherwise expressly set forth herein, shall be performed within the time frames and in accordance with the policies and procedures set forth in this Article a. QuantumShift shall submit to CenturyLink or, if so elected by QuantumShift to submit an annual data file as provided herein, its designated third party publisher (“Publisher”) all Listing Information (as hereinafter defined) relating to its subscribers (“Subscribers”) who desire published listings within a CenturyLink Directory. For purposes of this Agreement, “Listing Information” shall consist of the Subscriber’s name, address, telephone number, desired yellow pages classified heading (if any), and any other required listing information. Under no circumstances shall QuantumShift provide Subscriber data as a part of Listing Information for those Subscribers who do not desire published listings. Listing Information shall be supplied by QuantumShift without charge to CenturyLink. Listing Information shall be supplied, to CenturyLink, in a Local Service Request (“LSR”) or a standalone Directory Service Request (“DSR”) or, if to the Publisher, in a data file format as provided herein. Listing Information shall be submitted within the time frames as reasonably directed by CenturyLink and in accordance with established service guidelines in the CenturyLink Service Guide, which may be accessed at xxxx://xxxxxxxx.XxxxxxxXxxx.xxx//business/Wholesale/. Listing Information provided to CenturyLink via an LSR or DSR will be used by CenturyLink for purposes related to publishing directory listings. b. If providing Listing Information via an LSR or DSR, QuantumShift shall separately provide to CenturyLink Directory delivery address data for Subscribers, if different from the Listing Information, and for those Subscribers who do not desire published listings. Where QuantumShift elects to send an annual data file of Listing Information to the Publisher, QuantumShift shall provide a separate distribution file to the Publisher. c. If required for resolution of a Directory related inquiry, request or complaint received by QuantumShift from its Subscribers, QuantumShift shall promptly notify CenturyLink, but in any event within ten (10) days, of receipt of such inquiry, request, or complaint and shall reasonably cooperate with CenturyLink and Publisher to resolve such matters in a timely and expeditious manner. If the Parti...

Obligations and Responsibilities. (1) Prior to the Agreement being executed, the Sponsor will provide the Principal Investigator, and through the Principal Investigator the Institution and the Responsible HREC, with all current and relevant information regarding the Investigational Product as reasonably required to justify the nature, scope and duration of the Study. (2) The Sponsor will implement and maintain quality assurance and quality control systems with written standard operating procedures to ensure that the Study can be conducted and data generated, documented, recorded and reported in compliance with all of the documents referred to in clause 2. (3) The Sponsor will designate appropriately qualified personnel to advise on Study-related medical questions or problems. (4) The Sponsor will monitor the application of the Investigational Product in other places (both within and outside Australia) and advise the Institution, through the Principal Investigator and TGA of the cessation elsewhere of any relevant trial, or the withdrawal of the Investigational Product from any other market for safety reasons. (5) The Sponsor will notify the Institution of any Adverse Events (including Serious Adverse Events) that occur during the course of the Study (either at the Study Site or other study sites, including overseas sites) which may require alteration of the conduct of the Study, or which may affect the rights, interests, safety or well-being of Study Subjects. (6) The Sponsor will cooperate with the Institution and/or the Responsible HREC in investigating any Adverse Event (including Serious Adverse Event) arising out of or in connection with the Study. (7) To assist the Institution to comply with clause 8, the Sponsor will provide the Institution with adequate information and all necessary product accountability forms. (8) The Sponsor will provide indemnity to the Institution and members of the Responsible HREC against claims arising from the Study on the terms and conditions set out in the relevant Medicines Australia Form of Indemnity for Clinical Trials as set out in Schedule 3. (9) The Sponsor will comply with the Medicines Australia Guidelines for Compensation for Injury Resulting from Participation in a Company-sponsored Trial as specified in Schedule 5. (10) The Sponsor will maintain insurance with respect to its activities and indemnity obligations under this Agreement in accordance with Schedule 4. This insurance is to be evidenced by a certificate of currency of insurance, as re...

Obligations and Responsibilities. If the Principal Investigator leaves the Institution or otherwise ceases to be available, the Institution must consult with the Organisation and use reasonable endeavours to nominate as soon as practicable a replacement reasonably acceptable to both Parties. If the parties cannot agree on a replacement, either party may terminate this Agreement in accordance with clause 9.3. The Institution will not engage in any conduct on the Organisation’s behalf which is in violation of, or potentially in violation of, any applicable local laws or regulations. The Institution will make available adequate facilities, equipment and any other resource of the Institution reasonably required to safely follow the Protocol, provided that any amendments to the Protocol which take place after the execution of this Agreement and requiring any additional use of facilities, equipment, staff or resources, have been approved in writing by the Responsible HREC. The Institution will have an adequate number of appropriately qualified Personnel for the foreseen duration of the Research and ensure that such Personnel are adequately informed about the Protocol, Investigational Product(s), and their Research related duties and functions. The Institution will ensure that the Research is subject to the continuing oversight of the Responsible HREC throughout its conduct. PAYMENTS In consideration of the Institution conducting the Research, the Organisation will pay to the Institution as nominated in Schedule 2 in the manner and on the basis of the prices and at the times set out in Schedule 2. The prices set out in Schedule 2 do not include GST. At the time of payment, the Organisation must pay to the Institution any amount of GST that the Institution is required to pay in addition to the prices set out in Schedule 2, and in accordance with GST Law. Payments will be made by the Organisation upon either receipt of a valid tax invoice or a “Recipient Created Tax Invoice” issued by the Organisation, if applicable. the Organisation and the Institution warrant that they are registered under GST Law. Tax invoices must identify supplies for which GST is payable. PUBLICATIONS The Institution, Principal Investigator and other investigators (“Discloser”) involved in the Research have the right to Publish the methods, results of, and conclusions from, the Research. In any Publication referred to in clause 6.1 the Discloser will acknowledge the contribution of the Organisation. RESEARCH RESULTS AND INTEL...