Common use of Vlastnictví Clause in Contracts

Vlastnictví. All documents, protocols, data, know-how, methods, operations, formulas, Confidential Information and Materials (as defined below) provided to the Investigator pursuant to this Agreement are and shall remain Sponsor’s property. The completed CRFs, the final report (if applicable) and all information and data resulting from the Study including Study results (“Study Data”), shall also be owned by Sponsor. The Investigator assigns (and shall require all Study Team members to assign) to Sponsor all rights, title and interest, if any, in and to such Study Data. Sponsor shall not own subject medical records.

Appears in 2 contracts

Samples: Clinical Trial Agreement, Clinical Trial Agreement

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Vlastnictví. All documents, protocols, data, know-how, methods, operations, formulas, Confidential Information and Materials (as defined below) provided to the Investigator Provider pursuant to this Agreement are and shall remain Sponsor’s property. The completed CRFs, the final report (if applicable) and all information and data resulting from the Study Study, including Study results (“Study Data”), shall also be owned by Sponsor. The Investigator To the extent, if any, that the Provider has any rights, title and interest in the Study Data, Provider hereby assigns (and shall require to Sponsor, all Study Team members to assign) to Sponsor all such rights, title and interest, if any, in and to such Study Data. Sponsor shall not own subject medical records.

Appears in 2 contracts

Samples: Clinical Trial Agreement, Clinical Trial Agreement

Vlastnictví. All documents, protocols, data, know-how, methods, operations, formulas, Confidential Information and Materials (as defined below) provided to the Investigator Institution pursuant to this Agreement are and shall remain Sponsor’s property. The completed CRFs, the final report (if applicable) and all information and data resulting from the Study Study, including Study results (“Study Data”), shall also be owned by Sponsor. The Investigator Institution hereby assigns (and shall require all Study Team members to assign) to Sponsor Sponsor, all rights, title and interest, if any, in and to such Study Data. Sponsor shall not own subject medical records.

Appears in 2 contracts

Samples: Clinical Trial Agreement, Clinical Trial Agreement

Vlastnictví. All documents, protocols, data, know-how, methods, operations, formulas, Confidential Information and Materials (as defined below) provided to the Investigator pursuant to this Agreement are and shall remain Sponsor’s property. The completed CRFs, the final report (if applicable) and all information and data resulting from the Study including Study results (“Study Data”), shall also be owned by Sponsor. The Investigator assigns (and shall require all Study Team members to assign) to Sponsor all rights, title and interest, if any, in and to such Study Data. Sponsor shall not own subject Study Patient medical records.

Appears in 1 contract

Samples: Non Interventional Study Agreement

Vlastnictví. All documents, protocols, data, know-know- how, methods, operations, formulas, Confidential Information and Materials (as defined below) provided to the Investigator Site pursuant to this Agreement are and shall remain Sponsor’s property. The completed CRFs, the final report (if applicable) and all information and data resulting from the Study including Study results (“Study Data”), shall also be owned by Sponsor. The Investigator assigns (and shall require all Study Team members to assign) to Sponsor all rights, title and interest, if any, in and to such Study Data. Sponsor shall not own subject medical records.

Appears in 1 contract

Samples: Clinical Trial Agreement

Vlastnictví. All documents, protocols, data, know-know- how, methods, operations, formulas, Confidential Information and Materials (as defined below) provided to the Investigator pursuant to this Agreement are and shall remain Sponsor’s property. The completed CRFs, the final report (if applicable) and all information and data resulting from the Study including Study results (“Study Data”), shall also be owned by Sponsor. The Investigator assigns (and shall require all Study Team members to assign) to Sponsor all rights, title and interest, if any, in and to such Study Data. Sponsor shall not own subject medical records.

Appears in 1 contract

Samples: Clinical Trial Agreement

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Vlastnictví. All documents, protocols, data, know-how, methods, operations, formulas, Confidential Information and Materials (as defined below) provided to the Investigator pursuant to this Agreement are and shall remain Sponsor’s property. The completed CRFs, the final report (if applicable) and all information and data resulting from the Study including Study results (“Study Data”), shall also be owned by Sponsor. The Investigator assigns (and shall require all Study Team members to assign) to Sponsor all rights, title and interest, if any, in and to such Study Data. Sponsor shall not own Study subject medical records.

Appears in 1 contract

Samples: Clinical Trial Agreement

Vlastnictví. All documents, protocolsClinical Investigation Plan s, data, know-how, methods, operations, formulas, Confidential Information and Materials (as defined below) provided to the Investigator Institution pursuant to this Agreement are and shall remain Sponsor’s property. The completed CRFs, the final report (if applicable) and all information and data resulting from the Study Study, including Study results (“Study Data”), shall also be owned by Sponsor. The Investigator Site hereby assigns (and shall require all Study Team members to assign) to Sponsor Sponsor, all rights, title and interest, if any, in and to such Study Data. Sponsor shall not own any Study subject medical records.

Appears in 1 contract

Samples: Clinical Investigation Agreement

Vlastnictví. All documents, protocols, data, know-know- how, methods, operations, formulas, Confidential Information and Materials (as defined below) provided to the Investigator pursuant to this Agreement are and shall remain Sponsor’s property. The completed CRFs, the final report (if applicable) and all information and data resulting from the Study including Study results (“Study Data”), shall also be owned by Sponsor. The Investigator assigns (and shall require all Study Team members to assign) to Sponsor all rights, title and interest, if any, in and to such Study Data. Sponsor shall not own subject medical recordsrecords and other medical documentation; this is and will remain the property of the Institution even after the end of the Study.

Appears in 1 contract

Samples: Clinical Trial Agreement

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