Materials, Data and Information Transfer Sample Clauses
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Materials, Data and Information Transfer. Unless otherwise prohibited by applicable laws or contract, ▇▇▇▇▇▇ ▇▇▇▇▇▇▇ shall promptly return, transfer and assign to Palatin or its designee all materials relating to the Development and Commercialization of Products, including all Palatin Know-How in tangible form, all ▇▇▇▇▇▇ ▇▇▇▇▇▇▇ Know-How in tangible form, all Information, all Materials, all major regulatory submissions and other regulatory materials prepared by or on behalf of ▇▇▇▇▇▇ ▇▇▇▇▇▇▇ pursuant to the ▇▇▇▇▇▇ ▇▇▇▇▇▇▇ Development Plan, all Third Party agreements (provided that, to the extent required, the Third Party gives its prior written consent to the assignment of the relevant agreement to Palatin) and any other items relating to the Products, all of which shall be deemed confidential Information of Palatin (and not of ▇▇▇▇▇▇ ▇▇▇▇▇▇▇). For any of the foregoing documentation, data and information that is to be transferred to Palatin and is not in English, ▇▇▇▇▇▇ ▇▇▇▇▇▇▇ will, upon the request of Palatin, translate the foregoing into English and deliver true and accurate, in all material respects, translations thereof to Palatin. All such information shall be transferred to Palatin or its designee in an organized and clear manner, with all documents and files clearly labeled. Notwithstanding the foregoing, ▇▇▇▇▇▇ ▇▇▇▇▇▇▇ and/or ▇▇▇▇▇▇ ▇▇▇▇▇▇▇'▇ counsel may retain one (1) copy of tangible Palatin Know-How and ▇▇▇▇▇▇ ▇▇▇▇▇▇▇ Know-How for archival purposes and for ensuring compliance with Article 10 of the License Agreement.
Materials, Data and Information Transfer. Unless otherwise prohibited by applicable Law or contract, Takeda will, in accordance with the timing agreed upon by the Parties, promptly return, transfer and assign to ITI or its designee the agreed upon materials, including biological materials and samples, Information (including without limitation case report forms, study databases and other study records), Regulatory Materials, Regulatory Approvals, licenses, third party agreements and other items (including, without limitation, any Drug Master File(s), INDs, and NDAs, together with the material correspondence with Regulatory Authorities) related to the Compounds and Products and related data and Information relating to the Products and Compounds, all of which shall be deemed Confidential Information of ITI (and not of Takeda) (provided that Takeda will be allowed to retain (or if available, ask ITI to share in the future) any such materials that a Regulatory Authority requires Takeda to retain or submit under applicable Laws). For any of the foregoing documentation, data and information that is to be transferred to ITI and is not in English, Takeda will, upon the request of ITI, translate the foregoing into English and deliver true and accurate, in all material respects, translations thereof to ITI. All such information shall be transferred to ITI or its designee in an organized and clear manner, with all documents and files clearly labeled.