Common use of Use of Human Materials Clause in Contracts

Use of Human Materials. Without limiting Section 3.1, if any human cell lines, tissue, human clinical isolates or similar human-derived materials (“Human Materials”) have been or are to be collected and/or used in the Research Program, the Party using such Human Materials represents and warrants (i) that it has complied, and shall comply, with all applicable laws, guidelines and regulations relating to the collection and/or use of the Human Materials and (ii) that it has obtained, and shall obtain, all necessary approvals and appropriate informed consents, in writing, for the collection and/or use of such Human Materials. Each Party shall provide documentation of such approvals and consents to the other Party upon such other Party’s request. Each Party further represents and warrants that such Human Materials may be used as contemplated in this Agreement without any obligations to the individuals or entities (“Providers”) who contributed the Human Materials, including, without limitation, any obligations of compensation to such Providers.

Use of Human Materials. Without limiting Section 3.1, if If any human cell lines, tissue, human clinical isolates or similar human-derived materials (“Human Materials”"HUMAN MATERIALS") have been or are to be collected and/or used in the Research ProgramCollaboration, the each Party using such Human Materials represents and warrants (i) that it has complied, and or shall comply, with all applicable laws, guidelines and regulations relating to the collection and/or use of the Human Materials Materials, and (ii) that it has obtained, and or shall obtain, all necessary approvals and appropriate informed consents, in writing, for the collection and/or use of such Human Materials. Each Party shall provide documentation of such approvals and consents to upon the other Party upon such other Party’s 's request. Each Party further represents and warrants that such Human Materials may be used as contemplated in this Agreement without any obligations obligation to the individuals or entities (“Providers”"PROVIDERS") who contributed the Human Materials, including, without limitation, any obligations obligation of compensation to such ProvidersProviders or any other Third Party for the intellectual property associated with, or commercial use of, the Human Materials for any purposes.

Use of Human Materials. Without limiting Section 3.1, if If any human cell lines, tissue, human clinical isolates or similar human-derived materials (“Human Materials”) have been or are to be collected and/or used in the Initial Research Program, the Party using such Human Materials RENOVIS represents and warrants (i) that it has complied, and or shall comply, with all applicable laws, guidelines and regulations relating to the collection and/or use of the Human Materials and (ii) that it has obtained, and or shall obtain, all necessary approvals and appropriate informed consents, in writing, for the collection and/or use of such Human Materials. Each Party RENOVIS shall provide documentation of such approvals and consents to the other Party upon such other PartyMERCK’s request. Each Party RENOVIS further represents and warrants that such Human Materials may be used as contemplated in this Agreement without any obligations to the individuals or entities (“Providers”) who contributed the Human Materials, including, without limitation, any obligations of compensation to such ProvidersProviders or any other Third Party for the intellectual property associated with, or commercial use of, the Human Materials for any purposes.

Use of Human Materials. Without limiting Section 3.1, if If any human primary cell lines, human tissue, human clinical isolates or similar human-derived materials (“Human Materials”) have been or are to be collected and/or used in the Research ProgramProgram and Feasibility Studies, the each Party using such Human Materials represents and warrants (i) that it has complied, and or shall comply, with all applicable laws, guidelines and regulations relating to the collection and/or use of the Human Materials and (ii) that it has obtained, and or shall obtain, all necessary approvals and appropriate informed consents, in writing, for the collection and/or use of such Human Materials. Each Party shall provide documentation of such approvals and consents to the other Party upon such other PartyMerck’s request. Each Party further represents and warrants that such Human Materials may be used as contemplated in this Agreement without any obligations to the individuals or entities (“Providers”) who contributed the Human Materials, including, without limitation, any obligations of * Portions omitted pursuant to a request for confidential treatment and filed separately with the Securities and Exchange Commission. compensation to such ProvidersProviders or any other Third Party for the intellectual property associated with the Human Materials or the commercial use thereof for any purposes.

Use of Human Materials. Without limiting Section 3.1, if If any human cell lines, tissue, human clinical isolates or similar human-derived materials (“Human Materials”") have been or are to be collected and/or used in the Research ProgramDevelopment Program by a Party, the such Party using such Human Materials represents and warrants (i) that it has complied, and or shall comply, with all applicable laws, guidelines and regulations relating to the collection and/or use of the Human Materials and (ii) that it has obtained, and or shall obtain, all necessary approvals and appropriate informed consents, in writing, for the collection and/or use of such Human Materials. Each The Party using the Human Materials shall provide documentation of such approvals and consents to upon the other Party upon such other Party’s request. Each Party further represents and warrants that to its knowledge such Human Materials may be used as contemplated in this Agreement without any obligations to the individuals or entities (“Providers”") who contributed the Human Materials, including, without limitation, any obligations of compensation to such ProvidersProviders or any other Third Party for the intellectual property associated with, or commercial use of, the Human Materials for any purposes.

Use of Human Materials. Without limiting Section 3.1, if If any human cell lines, tissue, human clinical isolates or similar human-derived materials (“Human Materials”"HUMAN MATERIALS") have been or are to be collected and/or used in the Research Development Program, the Party using such Human Materials Nastech represents and warrants (i) that it has complied, and or shall comply, with all applicable laws, guidelines and regulations relating to the collection and/or use of the Human Materials and (ii) that it has obtained, and or shall obtain, all necessary approvals and appropriate informed consents, in writing, for the collection and/or use of such Human Materials. Each Party Nastech shall provide documentation of such approvals and consents to the other Party upon such other Party’s Merck's request. Each Party Nastech further represents and warrants that such Human Materials may be used as contemplated in this Agreement without any obligations to the individuals or entities (“Providers”"PROVIDERS") who contributed the Human Materials, including, without limitation, any obligations of compensation to such ProvidersProviders or any other Third Party for the intellectual property associated with, or commercial use of, the Human Materials for any purposes.

Use of Human Materials. Without limiting Section 3.1, if With respect to any human cell lines, tissue, human clinical isolates or similar human-derived materials (“Human Materials”) that have been or are to be collected and/or used in the Research ProgramProgram ("Human Materials"), the each Party using such Human Materials represents and warrants (i) that it has complied, and or shall comply, with all applicable laws, guidelines and regulations relating to the collection and/or use of the Human Materials and (ii) that it has obtained, and or shall obtain, all necessary approvals and appropriate informed consents, in writing, for the collection and/or use of such Human Materials. Each Party deCODE shall provide documentation of such approvals and consents to the other Party upon such other Party’s MERCK's request. Each Party further represents and warrants that such Human Materials may be used as contemplated in this Agreement without any obligations to the individuals or entities (“"Providers”") who contributed the Human Materials, including, without limitation, any obligations of compensation to such ProvidersProviders or any other Third Party for the intellectual property associated with, or commercial use of, the Human Materials for any purposes.

Use of Human Materials. Without limiting Section 3.1, if If any human primary cell lines, human tissue, human clinical isolates or similar human-derived materials (“Human Materials”"HUMAN MATERIALS") have been or are to be collected and/or used in the Research Program, the Party using such Human Materials Idera represents and warrants (i) that it has complied, and or shall comply, with all applicable laws, guidelines and regulations relating to the collection and/or use of the Human Materials and (ii) that it has obtained, and or shall obtain, all necessary approvals and appropriate informed consents, in writing, for the collection and/or use of such Human Materials. Each Party Idera shall provide documentation of such approvals and consents to the other Party upon such other Party’s Merck's request. Each Party Idera further represents and warrants that such Human Materials may be used as contemplated in this Agreement without any obligations to the individuals or entities (“Providers”"PROVIDERS") who contributed the Human Materials, including, without limitation, any obligations of compensation to such ProvidersProviders or any other Third Party for the intellectual property associated with the Human Materials or the commercial use thereof for any purposes.

Use of Human Materials. Without limiting Section 3.1, if With respect to any human cell lines, tissue, human clinical isolates or similar human-derived materials (“Human Materials”) that have been or are to be collected and/or used in the Research ProgramProgram (“Human Materials”), the each Party using such Human Materials represents and warrants (i) that it has complied, and or shall comply, with all applicable laws, guidelines and regulations relating to the collection and/or use of the Human Materials and (ii) that it has obtained, and or shall obtain, all necessary approvals and appropriate informed consents, in writing, for the collection and/or use of such Human Materials. Each Party deCODE shall provide documentation of such approvals and consents to the other Party upon such other PartyMERCK’s request. Each Party further represents and warrants that such Human Materials may be used as contemplated in this Agreement without any obligations to the individuals or entities (“Providers”) who contributed the Human Materials, including, without limitation, any obligations of compensation to such ProvidersProviders or any other Third Party for the intellectual property associated with, or commercial use of, the Human Materials for any purposes.