{"component": "clause", "props": {"groups": [{"snippet_links": [{"key": "the-parties-agree-that", "type": "clause", "offset": [0, 22]}, {"key": "eligible-students", "type": "clause", "offset": [58, 75]}, {"key": "in-district", "type": "definition", "offset": [145, 156]}, {"key": "parent-or-legal-guardian", "type": "definition", "offset": [177, 201]}, {"key": "use-under-this-agreement", "type": "clause", "offset": [282, 306]}, {"key": "exhibit-a", "type": "definition", "offset": [371, 380]}, {"key": "responsible-for", "type": "clause", "offset": [415, 430]}, {"key": "students-enrolled", "type": "definition", "offset": [445, 462]}, {"key": "a-copy-of", "type": "clause", "offset": [527, 536]}, {"key": "to-corporation", "type": "clause", "offset": [565, 579]}, {"key": "the-provision-of-services", "type": "clause", "offset": [589, 614]}, {"key": "district-shall", "type": "clause", "offset": [620, 634]}, {"key": "original-copy", "type": "clause", "offset": [648, 661]}], "snippet": "The Parties agree that Services shall be provided only to Eligible Students. \u201cEligible Students\u201d are defined herein as students who are enrolled in District\u2019s Schools and whose parent or legal guardian, as appropriate, have completed the Consent Form. The Consent Form approved for use under this Agreement shall be substantially in the form attached and incorporated as Exhibit A (\u201cConsent Form\u201d). The District is responsible for providing all students enrolled in its Schools with the Consent Form. The District will provide a copy of all completed Consent Forms to Corporation prior to the provision of Services. The District shall maintain the original copy of all completed Consent Forms.", "samples": [{"hash": "jlK8QBvyTFD", "uri": "/contracts/jlK8QBvyTFD#consent-forms", "label": "Affiliation Agreement", "score": 31.9937820435, "published": true}, {"hash": "74XU0cR4Lpp", "uri": "/contracts/74XU0cR4Lpp#consent-forms", "label": "Affiliation Agreement", "score": 28.0370407104, "published": true}], "size": 2, "hash": "f6fee7f27123f1241d5686c781f7efaa", "id": 6}, {"snippet_links": [{"key": "provide-the", "type": "clause", "offset": [0, 11]}, {"key": "reviewing-irb", "type": "definition", "offset": [12, 25]}, {"key": "the-site", "type": "clause", "offset": [31, 39]}, {"key": "information-requested", "type": "clause", "offset": [49, 70]}, {"key": "consent-form", "type": "definition", "offset": [134, 146]}, {"key": "approval-by", "type": "clause", "offset": [163, 174]}, {"key": "written-informed-consent", "type": "clause", "offset": [199, 223]}, {"key": "relying-institution", "type": "definition", "offset": [286, 305]}, {"key": "change-to", "type": "clause", "offset": [423, 432]}, {"key": "approval-of", "type": "clause", "offset": [466, 477]}], "snippet": "Provide the Reviewing IRB with the site-specific information requested/identified in the customizable sections of the Reviewing IRB\u2019s consent form, for review and approval by the Reviewing IRB, when written informed consent is required. Once the consent form is approved for use by the Relying Institution/Site Investigator(s), the Relying Institution will not, and will require that its Site Investigator(s) not, make any change to the form without obtaining prior approval of that change from the Reviewing IRB.", "samples": [{"hash": "eYBYrxOzznh", "uri": "/contracts/eYBYrxOzznh#consent-forms", "label": "Master Common Reciprocal Institutional Review Board Authorization Agreement", "score": 26.3702945709, "published": true}, {"hash": "bS0b6SNB52q", "uri": "/contracts/bS0b6SNB52q#consent-forms", "label": "Master Common Reciprocal Institutional Review Board Authorization Agreement", "score": 26.2799453735, "published": true}, {"hash": "ic7YlNFiWNO", "uri": "/contracts/ic7YlNFiWNO#consent-forms", "label": "Master Common Reciprocal Institutional Review Board Authorization Agreement", "score": 24.4373722076, "published": true}], "size": 5, "hash": "c69818e67e7a4cec8d23ccfc12ad2d0f", "id": 1}, {"snippet_links": [{"key": "user-shall", "type": "definition", "offset": [9, 19]}, {"key": "waiver-of-liability", "type": "definition", "offset": [41, 60]}, {"key": "the-event", "type": "clause", "offset": [91, 100]}, {"key": "medical-treatment", "type": "definition", "offset": [191, 208]}, {"key": "parent-or-legal-guardian", "type": "definition", "offset": [239, 263]}, {"key": "completed-forms", "type": "clause", "offset": [298, 313]}, {"key": "by-facility", "type": "clause", "offset": [332, 343]}, {"key": "to-university", "type": "clause", "offset": [368, 381]}, {"key": "upon-request", "type": "definition", "offset": [382, 394]}], "snippet": "Facility User shall obtain a consent and waiver of liability form for each minor attending the Event, which authorizes Facility User\u2019s employees or staff to take ill or injured attendees for medical treatment. Forms shall be signed by the parent or legal guardian of any minor attending the Event. Completed forms shall be retained by Facility User and made available to University upon request.", "samples": [{"hash": "58fySEeQf2W", "uri": "/contracts/58fySEeQf2W#consent-forms", "label": "Facility Use Agreement", "score": 20.5776863098, "published": true}, {"hash": "bF1x52RNRTE", "uri": "/contracts/bF1x52RNRTE#consent-forms", "label": "Facility Use Agreement", "score": 18.5872688293, "published": true}, {"hash": "7Lv2W3rfOJa", "uri": "/contracts/7Lv2W3rfOJa#consent-forms", "label": "Facility Use Agreement", "score": 18.566734314, "published": true}], "size": 5, "hash": "d5dbfe0d17ad9baac9206a77c2dd6ddc", "id": 2}, {"snippet_links": [{"key": "relying-institution", "type": "definition", "offset": [16, 35]}, {"key": "informed-consent-forms", "type": "clause", "offset": [61, 83]}, {"key": "the-research", "type": "clause", "offset": [95, 107]}, {"key": "reviewing-irb", "type": "definition", "offset": [118, 131]}, {"key": "generally-the", "type": "clause", "offset": [318, 331]}, {"key": "availability-of", "type": "clause", "offset": [348, 363]}, {"key": "for-research", "type": "clause", "offset": [391, 403]}, {"key": "costs-incurred", "type": "definition", "offset": [457, 471]}, {"key": "approval-by", "type": "clause", "offset": [547, 558]}, {"key": "provide-a", "type": "definition", "offset": [594, 603]}], "snippet": "Provide to each Relying Institution and Site Investigator(s) informed consent forms to use for the Research where the Reviewing IRB has determined that such a consent form(s) is required. The Reviewing IRB will permit a Relying Institution/Site Investigator(s) to customize limited site-specific sections of the form, generally the sections on the availability of treatment and compensation for research-related injury; payment or reimbursement of research costs incurred by subjects; and local contacts. Any such modifications will be subject to approval by the Reviewing IRB, which will then provide a final approved consent form(s) to the Relying Institution(s)/Site Investigator(s) for use.", "samples": [{"hash": "eYBYrxOzznh", "uri": "/contracts/eYBYrxOzznh#consent-forms", "label": "Master Common Reciprocal Institutional Review Board Authorization Agreement", "score": 26.3702945709, "published": true}, {"hash": "bS0b6SNB52q", "uri": "/contracts/bS0b6SNB52q#consent-forms", "label": "Master Common Reciprocal Institutional Review Board Authorization Agreement", "score": 26.2799453735, "published": true}, {"hash": "ic7YlNFiWNO", "uri": "/contracts/ic7YlNFiWNO#consent-forms", "label": "Master Common Reciprocal Institutional Review Board Authorization Agreement", "score": 24.4373722076, "published": true}], "size": 4, "hash": "9797f490578910d3ac873a6da6dec066", "id": 3}, {"snippet_links": [{"key": "informed-consent-form", "type": "definition", "offset": [29, 50]}, {"key": "in-consultation-with", "type": "definition", "offset": [78, 98]}, {"key": "changes-to", "type": "clause", "offset": [112, 122]}, {"key": "model-form", "type": "definition", "offset": [128, 138]}, {"key": "relate-to", "type": "definition", "offset": [144, 153]}, {"key": "the-product", "type": "clause", "offset": [154, 165]}, {"key": "subject-to", "type": "clause", "offset": [175, 185]}, {"key": "written-consent", "type": "definition", "offset": [196, 211]}, {"key": "will-provide", "type": "clause", "offset": [279, 291]}, {"key": "written-explanation", "type": "clause", "offset": [311, 330]}, {"key": "after-receiving", "type": "clause", "offset": [405, 420]}, {"key": "authorizations-and-consents", "type": "clause", "offset": [472, 499]}, {"key": "in-connection-with", "type": "clause", "offset": [593, 611]}, {"key": "in-accordance-with", "type": "definition", "offset": [643, 661]}, {"key": "eu-data-protection-directive", "type": "definition", "offset": [673, 701]}, {"key": "applicable-law", "type": "clause", "offset": [723, 737]}, {"key": "clinical-trial-data", "type": "definition", "offset": [754, 773]}, {"key": "this-agreement", "type": "clause", "offset": [806, 820]}], "snippet": "OV shall prepare the patient informed consent form for the mBC Clinical Trial in consultation with R-Pharm. Any changes to such model form that relate to the Product shall be subject to R-Pharm\u2019s written consent, not to be unreasonably withheld, conditioned, or delayed. R-Pharm will provide such consent, or a written explanation for why such consent is being withheld, within fifteen (15) Business Days after receiving OV\u2019s request therefor. OV shall obtain all patient authorizations and consents for the mBC Clinical Trial, and OV shall ensure that all patient authorizations and consents in connection with the mBC Clinical Trial permit, in accordance with HIPAA, the EU Data Protection Directive or any other similar Applicable Law, sharing of mBC Clinical Trial Data with R-Pharm in accordance with this Agreement.", "samples": [{"hash": "k45HzhhA3yp", "uri": "/contracts/k45HzhhA3yp#consent-forms", "label": "Development, Option and License Agreement (Allarity Therapeutics, Inc.)", "score": 32.7946624756, "published": true}, {"hash": "fnb6CjlSaTE", "uri": "/contracts/fnb6CjlSaTE#consent-forms", "label": "Development, Option and License Agreement (Allarity Therapeutics, Inc.)", "score": 32.6331291199, "published": true}], "size": 2, "hash": "1e481517d3b4dd3a678789b19544200a", "id": 4}, {"snippet_links": [{"key": "licensee-shall", "type": "clause", "offset": [0, 14]}, {"key": "waiver-of-liability", "type": "definition", "offset": [36, 55]}, {"key": "the-event", "type": "clause", "offset": [86, 95]}, {"key": "medical-treatment", "type": "definition", "offset": [181, 198]}, {"key": "parent-or-legal-guardian", "type": "definition", "offset": [229, 253]}, {"key": "completed-forms", "type": "clause", "offset": [288, 303]}, {"key": "by-licensee", "type": "clause", "offset": [322, 333]}, {"key": "to-university", "type": "clause", "offset": [353, 366]}, {"key": "upon-request", "type": "definition", "offset": [367, 379]}, {"key": "responsible-for", "type": "clause", "offset": [425, 440]}, {"key": "plans-for", "type": "clause", "offset": [466, 475]}, {"key": "agrees-to", "type": "clause", "offset": [630, 639]}, {"key": "in-favor-of", "type": "definition", "offset": [688, 699]}, {"key": "the-university", "type": "definition", "offset": [700, 714]}, {"key": "related-to", "type": "definition", "offset": [715, 725]}, {"key": "risk-of-exposure", "type": "clause", "offset": [730, 746]}, {"key": "communicable-disease", "type": "definition", "offset": [768, 788]}], "snippet": "Licensee shall obtain a consent and waiver of liability form for each minor attending the Event, which authorizes Licensee\u2019s employees or staff to take ill or injured attendees for medical treatment. Forms shall be signed by the parent or legal guardian of any minor attending the Event. Completed forms shall be retained by Licensee and made available to University upon request. Licensee understands that University is not responsible for ensuring that Licensee\u2019s plans for the Event meet the guidance published by the CDC and MDH, nor is University responsible for ensuring Licensee adheres to its plans. Licensee specifically agrees to obtain a waiver of liability from each attendee in favor of the University related to the risk of exposure to COVID-19 or other communicable disease and the risk that an attendee may spread disease to others.", "samples": [{"hash": "5szrDHSVWLR", "uri": "/contracts/5szrDHSVWLR#consent-forms", "label": "Safety of Minors Addendum", "score": 31.2636221621, "published": true}, {"hash": "gkzCKLUxKeA", "uri": "/contracts/gkzCKLUxKeA#consent-forms", "label": "Facility Use Agreement", "score": 30.2242603302, "published": true}], "size": 2, "hash": "c78a0ca51e0ebcf94514eb13d7dd08f1", "id": 5}, {"snippet_links": [{"key": "as-directed", "type": "definition", "offset": [0, 11]}, {"key": "by-practice", "type": "clause", "offset": [12, 23]}, {"key": "complete-the", "type": "clause", "offset": [25, 37]}, {"key": "necessary-for", "type": "definition", "offset": [55, 68]}, {"key": "client-consent", "type": "definition", "offset": [79, 93]}, {"key": "the-content", "type": "clause", "offset": [125, 136]}, {"key": "communication-of", "type": "clause", "offset": [216, 232]}, {"key": "clinical-information", "type": "definition", "offset": [233, 253]}, {"key": "responsibility-of", "type": "clause", "offset": [285, 302]}, {"key": "licensed-contractors", "type": "clause", "offset": [320, 340]}], "snippet": "As directed by Practice, complete the clerical aspects necessary for preparing client consent forms; provided, however, that the content of such forms shall be determined by Practice, and provided, further, that the communication of clinical information to clients shall solely be the responsibility of Practice and the Licensed Contractors;", "samples": [{"hash": "kT90Q7YWAfR", "uri": "/contracts/kT90Q7YWAfR#consent-forms", "label": "Management Services Agreement (Nava Health Md, LLC)", "score": 33.8186187744, "published": true}, {"hash": "3Jw5cFOz8zi", "uri": "/contracts/3Jw5cFOz8zi#consent-forms", "label": "Management Services Agreement (99 Acquisition Group Inc.)", "score": 33.3162231445, "published": true}], "size": 2, "hash": "627233068727dd8909e424b5f0b74793", "id": 7}, {"snippet_links": [{"key": "notice-to", "type": "definition", "offset": [27, 36]}, {"key": "subject-to", "type": "clause", "offset": [91, 101]}, {"key": "substance-testing", "type": "definition", "offset": [177, 194]}], "snippet": "Subcontractor must provide notice to and obtain signed consents from its personnel who are subject to these requirements to release to JCI, at JCI\u2019s request, the results of any Substance Testing performed.", "samples": [{"hash": "2Ya33LpYBep", "uri": "/contracts/2Ya33LpYBep#consent-forms", "label": "Subcontract", "score": 35.7785301208, "published": true}], "size": 2, "hash": "db17491c4ec70c05e566b69c8466219c", "id": 8}, {"snippet_links": [{"key": "specific-consent", "type": "definition", "offset": [5, 21]}, {"key": "approved-model", "type": "definition", "offset": [38, 52]}, {"key": "irb-of-record", "type": "clause", "offset": [70, 83]}, {"key": "local-context", "type": "definition", "offset": [105, 118]}, {"key": "a-or-b", "type": "clause", "offset": [145, 151]}, {"key": "reviewed-by", "type": "definition", "offset": [178, 189]}, {"key": "prior-to", "type": "definition", "offset": [210, 218]}, {"key": "the-sponsor", "type": "clause", "offset": [230, 241]}, {"key": "for-approval", "type": "definition", "offset": [242, 254]}, {"key": "to-ensure", "type": "clause", "offset": [255, 264]}, {"key": "required-language", "type": "clause", "offset": [265, 282]}], "snippet": "\u2610\u0001MH Specific consent/assent form(s) [approved model consent from the IRB of Record] tracked with the MH local context information (See Appendix A or B). The ICF will need to be reviewed by the MetroHealth IRB PRIOR to sending to the sponsor for approval to ensure required language is present.", "samples": [{"hash": "bDU5wSbIORS", "uri": "/contracts/bDU5wSbIORS#consent-forms", "label": "Reliance Agreement", "score": 35.1111297607, "published": true}], "size": 2, "hash": "38ccf755cb12ba6771e974cae17b7f9a", "id": 9}, {"snippet_links": [{"key": "relying-institution", "type": "definition", "offset": [16, 35]}, {"key": "informed-consent-forms", "type": "clause", "offset": [61, 83]}, {"key": "the-research", "type": "clause", "offset": [95, 107]}, {"key": "reviewing-irb", "type": "definition", "offset": [118, 131]}, {"key": "generally-the", "type": "clause", "offset": [318, 331]}, {"key": "availability-of", "type": "clause", "offset": [348, 363]}, {"key": "for-research", "type": "clause", "offset": [391, 403]}, {"key": "costs-incurred", "type": "definition", "offset": [457, 471]}, {"key": "approval-by", "type": "clause", "offset": [547, 558]}, {"key": "provide-a", "type": "definition", "offset": [594, 603]}, {"key": "conflicts-of-interest", "type": "definition", "offset": [695, 716]}, {"key": "conflict-of-interest", "type": "definition", "offset": [742, 762]}, {"key": "interest-determinations", "type": "clause", "offset": [832, 855]}, {"key": "management-plans", "type": "definition", "offset": [871, 887]}, {"key": "by-non", "type": "clause", "offset": [897, 903]}, {"key": "section-66", "type": "clause", "offset": [945, 956]}, {"key": "with-respect-to", "type": "clause", "offset": [964, 979]}, {"key": "overall-pi", "type": "definition", "offset": [984, 994]}, {"key": "research-personnel", "type": "definition", "offset": [1028, 1046]}, {"key": "in-connection-with", "type": "clause", "offset": [1047, 1065]}, {"key": "continuing-review", "type": "clause", "offset": [1171, 1188]}, {"key": "without-limiting-the-foregoing", "type": "clause", "offset": [1232, 1262]}, {"key": "required-by", "type": "definition", "offset": [1297, 1308]}, {"key": "the-plan", "type": "clause", "offset": [1309, 1317]}, {"key": "the-relevant", "type": "clause", "offset": [1421, 1433]}, {"key": "authority-to", "type": "definition", "offset": [1485, 1497]}, {"key": "additional-prohibitions", "type": "clause", "offset": [1505, 1528]}, {"key": "management-requirements", "type": "definition", "offset": [1541, 1564]}, {"key": "more-stringent", "type": "definition", "offset": [1565, 1579]}, {"key": "a-non", "type": "clause", "offset": [1612, 1617]}, {"key": "to-approve", "type": "clause", "offset": [1659, 1669]}, {"key": "not-modify", "type": "clause", "offset": [1726, 1736]}, {"key": "mandated-disclosure", "type": "clause", "offset": [1770, 1789]}, {"key": "acceptance-by-the", "type": "clause", "offset": [1830, 1847]}, {"key": "extraordinary-circumstance", "type": "definition", "offset": [1876, 1902]}, {"key": "the-non", "type": "clause", "offset": [2092, 2099]}, {"key": "ceded-review", "type": "definition", "offset": [2371, 2383]}, {"key": "approval-or-disapproval", "type": "clause", "offset": [2400, 2423]}, {"key": "notification-of", "type": "definition", "offset": [2796, 2811]}, {"key": "notify-the", "type": "clause", "offset": [2865, 2875]}, {"key": "required-modifications", "type": "definition", "offset": [3054, 3076]}, {"key": "changes-in", "type": "clause", "offset": [3082, 3092]}, {"key": "approved-by", "type": "definition", "offset": [3119, 3130]}, {"key": "initial-approval", "type": "definition", "offset": [3155, 3171]}, {"key": "corrective-action-plans", "type": "clause", "offset": [3222, 3245]}, {"key": "participating-institutions", "type": "clause", "offset": [3336, 3362]}], "snippet": "Provide to each Relying Institution and Site Investigator(s) informed consent forms to use for the Research where the Reviewing IRB has determined that such a consent form(s) is required. The Reviewing IRB will permit a Relying Institution/Site Investigator(s) to customize limited site-specific sections of the form, generally the sections on the availability of treatment and compensation for research-related injury; payment or reimbursement of research costs incurred by subjects; and local contacts. Any such modifications will be subject to approval by the Reviewing IRB, which will then provide a final approved consent form(s) to the Relying Institution(s)/Site Investigator(s) for use. Conflicts of Interest. Consider any applicable conflict of interest assurances received from federal Relying Institutions or conflict of interest determinations and associated management plans provided by non-federal Relying Institutions pursuant to Section 6.6 hereof with respect to the Overall PI, Site Investigator(s), and other Research Personnel in connection with the Research. The Reviewing IRB will ensure that any management plan is incorporated into its initial or continuing review or other deliberations, as applicable, and without limiting the foregoing, that any disclosures to subjects required by the plan and that are approvable by the Reviewing IRB are included in the approved informed consent form(s) for the relevant Relying Institution. The Reviewing IRB retains the authority to impose additional prohibitions or conflict management requirements more stringent or restrictive than proposed by a non-federal Relying Institution if necessary to approve the Research, provided, however, the Reviewing IRB will not modify or change any management plan or mandated disclosure to subjects without discussion with and acceptance by the Relying Institution. In the extraordinary circumstance that the Reviewing IRB is unable to implement/approve a non-federal Relying Institution\u2019s prohibitions or management plans, the Reviewing IRB will so inform such Relying Institution or, if the non-federal Relying Institution fails to accept any additional prohibitions or requirements, the non-federal Relying Institution will so inform the Reviewing IRB. If the institutions are not able to identify a mutually agreeable approach, the Research will be withdrawn from Ceded Review (without an IRB approval or disapproval) with respect to that non-federal Relying Institution. If the Reviewing IRB concludes that it cannot rely upon the assurances from a federal Relying Institution, the Reviewing IRB will so inform the federal Relying Institution, and the Research will be withdrawn from Ceded Review (without an IRB approval or disapproval) with respect to that federal Relying Institution. Notification of IRB Decisions, Changes, Lapses in Approval. Promptly notify the Overall PI, Site Investigator(s), and the Relying Institution(s) of its determinations (e.g., exemption) or review decisions regarding the Research (e.g., approval, disapproval, required modifications); of changes in the Research reviewed and approved by the Reviewing IRB after initial approval; and of lapses in IRB approval and any applicable corrective action plans. Such notification may be made through the Reviewing IRB\u2019s designee, as determined by the Participating Institutions in connection with the specific Research.", "samples": [{"hash": "dZ4j3MiO97O", "uri": "/contracts/dZ4j3MiO97O#consent-forms", "label": "Master Common Reciprocal Institutional Review Board Authorization Agreement", "score": 26.5017108917, "published": true}], "size": 2, "hash": "816a8e1f7f76f8f09f0f37fcf2c8a0d6", "id": 10}], "next_curs": "ClYSUGoVc35sYXdpbnNpZGVyY29udHJhY3RzcjILEhZDbGF1c2VTbmlwcGV0R3JvdXBfdjU2IhZjb25zZW50LWZvcm1zIzAwMDAwMDBhDKIBAmVuGAAgAA==", "clause": {"children": [], "size": 37, "title": "Consent Forms", "parents": [["responsibilities-of-the-relying-institutions", "Responsibilities of the Relying Institution(s"], ["administrative-services", "Administrative Services"], ["substance-testing", "Substance Testing"], ["development-and-regulatory", "Development and Regulatory"], ["health-services", "Health Services"]], "id": "consent-forms", "related": [["assignment-form", "ASSIGNMENT FORM", "ASSIGNMENT FORM"], ["payment-for-consent", "Payment for Consent", "Payment for Consent"], ["vendor-agreement-signature-form", "Vendor Agreement Signature Form", "Vendor Agreement Signature Form"], ["payment-for-consents", "Payment for Consents", "Payment for Consents"], ["scope-of-consent", "Scope of Consent", "Scope of Consent"]], "related_snippets": [], "updated": "2025-07-26T06:10:53+00:00"}, "json": true, "cursor": ""}}