Additional Research. Institution and Principal Investigator shall not conduct any research nor facilitate third parties to conduct any research not required by the Protocol on (i) Study Subjects during the Study (including any additional research technique, procedure, questionnaire, or observation), or (ii) the data derived from the Study, each of (i), (ii), and (iii) without the prior written consent of CRO or ▇▇▇▇▇▇▇. Hereinafter, the research described in the previous sentence shall be referred to as “Additional Research”. In any case where CRO or Janssen gives such approval, the approved Additional Research shall be considered either an amendment to the original Protocol or shall be the subject of another written agreement between ▇▇▇▇▇▇▇, CRO and Institution and Principal Investigator. Institution and Principal Investigator shall conduct all Additional Research in compliance with all applicable regulations, including requirements for obtaining appropriate EC approval and subject informed consent. Without limiting any other remedy available by law to Janssen, if Institution and/or Principal Investigator conducts Additional Research in breach of this section, and such Additional Research results in an Invention (as defined in Section 8 below), Institution and Principal Investigator (as applicable) hereby grant to Janssen or its designee an irrevocable, worldwide, paid up, royalty-free, exclusive license, with right of sub-license, to make, have made, use, have used, sell, have sold, and import any such invention that results from such Additional Research. This Section shall survive termination or expiration of this Agreement.
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Additional Research. Institution and Principal Investigator shall not conduct any research nor facilitate third parties to conduct any research not required by the Protocol on (i) Study Subjects during the Study (including any additional research technique, procedure, questionnaire, or observation), or (ii) the data derived from the Study, each of (i), (ii), and (iii) without the prior written consent of CRO or ▇▇▇▇▇▇▇Janssen. Hereinafter, the research described in the previous sentence shall be referred to as “Additional Research”. In any case where CRO or Janssen gives such approval, the approved Additional Research shall be considered either an amendment to the original Protocol or shall be the subject of another written agreement between ▇▇▇▇▇▇▇Janssen, CRO and Institution and Principal Investigator. Institution and Principal Investigator shall conduct all Additional Research in compliance with all applicable regulations, including requirements for obtaining appropriate EC approval and subject informed consent. Without limiting any other remedy available by law to Janssen, if Institution and/or Principal Investigator conducts Additional Research in breach of this section, and such Additional Research results in an Invention (as defined in Section 8 below), Institution and Principal Investigator (as applicable) hereby grant to Janssen or its designee an irrevocable, worldwide, paid up, royalty-free, exclusive license, with right of sub-license, to make, have made, use, have used, sell, have sold, and import any such invention that results from such Additional Research. This Section shall survive termination or expiration of this Agreement.have
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