Material Transfer Provisions Sample Clauses

Material Transfer Provisions. Where the Protocol requires the Participating Organisation to supply Material to the Sponsor this Appendix 4 shall apply. [DELETE IF NOT APPLICABLE] In accordance with the Protocol, the Participating Organisation shall send Material to the Sponsor or, in accordance with Section 7 below, to a third party nominated by the Sponsor; The Participating Organisation warrants that all Material has been collected with appropriate informed consent and has been collected and handled in accordance with applicable law (including, without limitation, the Human Tissue Act 2004) and as required by the Protocol; Subject to Section 2 above, the Material is supplied without any warranty, expressed or implied, including as to its properties, merchantable quality, fitness for any particular purpose, or freedom from infection; The Sponsor shall ensure, or procure through an agreement with the Sponsor’s nominee as stated in item 1 above, that: the Material is used in accordance with the consent of the Non-Interventional Study Subject and the approval of all Regulatory Authorities for the Non-Interventional Study and the Protocol; the Material is handled and stored in accordance with applicable law; the Material shall not be redistributed or released to any person other than in accordance with the Protocol or for the purpose of undertaking other research approved by an appropriate ethics committee and in accordance with the Non-Interventional Study Subject’s consent. The Parties shall comply with all relevant laws, regulations and codes of practice governing the Non-Interventional Study and the use of human biological material; The Participating Organisation and the Sponsor shall each be responsible for keeping a record of the Material that has been transferred according to this Appendix 4; To the extent permitted by law, the Participating Organisation and its Personnel shall not be liable for any consequences of the supply to or the use by the Sponsor of the Material, or of the supply to or the use by any third party to whom the Sponsor subsequently provides the Material, or the Sponsor’s nominee as stated in Section 1 above, save to the extent that any liability that arises is a result of the negligence, wrongful acts or omissions or breach of statutory duty of the Participating Organisation or its Personnel, or their failure to comply with the terms of this Agreement; The Sponsor undertakes that, in the event that Material is provided to a third party in accordance with Sectio...
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Material Transfer Provisions. 1. Where the Protocol requires the Trust to supply Material to the Sponsor / Affiliate, this Appendix 6 shall apply.
Sample 1
Material Transfer Provisions. Where the Clinical Investigation Plan requires the Trial Site to supply Material to the Sponsor or CRO this Appendix 6 shall apply. [DELETE IF NOT APPLICABLE] In accordance with the Clinical Investigation Plan, the Trial Site shall send Material to the Sponsor, CRO or, in accordance with Section 7 below, to a third party nominated by the Sponsor or CRO. The Trial Site warrants that all Material has been collected with appropriate informed consent and has been collected and handled in accordance with applicable law (including, without limitation, the Human Tissue Act 2004) and as required by the Clinical Investigation Plan. Subject to Section 2 above, the Material is supplied without any warranty, expressed or implied, including as to its properties, merchantable quality, fitness for any particular purpose, or freedom from infection. The Sponsor or CRO shall ensure, or procure through an agreement with the nominee of the Sponsor or CRO as stated in item 1 above, that: the Material is used in accordance with the consent of the Clinical Investigation Subject and the approval of all Regulatory Authorities for the Clinical Investigation and the Clinical Investigation Plan; the Material is handled and stored in accordance with applicable law; the Material shall not be redistributed or released to any person other than in accordance with the Clinical Investigation Plan or for the purpose of undertaking other research approved by an appropriate ethics committee and in accordance with the Clinical Investigation Subject’s consent. The Parties shall comply with all relevant laws, regulations and codes of practice governing the Clinical Investigation and the use of human biological material. The Trial Site and the Sponsor or CRO shall each be responsible for keeping a record of the Material that has been transferred according to this Appendix 6. To the extent permitted by law, the Trial Site and its Personnel shall not be liable for any consequences of the supply to or the use by the Sponsor or CRO of the Material, or of the supply to or the use by any third party to whom the Sponsor or CRO subsequently provides the Material, or the nominee of the Sponsor or CRO as stated in Section 1 above, save to the extent that any liability that arises is a result of the negligence, wrongful acts or omissions or breach of statutory duty of the Trial Site or its Personnel, or their failure to comply with the terms of this Agreement. The Sponsor and/or undertakes that, in the event...
Sample 1
Material Transfer Provisions. Where the Protocol requires the Trust to supply Material to the Sponsor / Affiliate, this Appendix 6 shall apply. In accordance with the Protocol, the Trust shall send Material to the Sponsor / Affiliate or, in accordance with provision 8 below, to a third party nominated by the Sponsor / Affiliate. The Trust warrants that all Material has been collected with appropriate informed consent and has been collected and handled in accordance with applicable law (including, without limitation, the Human Tissue Xxx 0000 or the Human Tissue Act (Scotland) Act 2006 (as the case may be) and as required by the Protocol. Subject to provision 3 above, the Materials are supplied without any warranty, expressed or implied, including as to their properties, merchantable quality, fitness for any particular purpose, or freedom from infection. The Sponsor / Affiliate shall ensure, or procure through an agreement with the Sponsor’s / Affiliate’s nominee as stated in provision 2 above that:
Sample 1
Material Transfer Provisions. 10. The following provisions shall apply in respect of any Transfer of Material from the Provider to the Recipient:
Sample 1

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