Common use of Use of Study Results Clause in Contracts

Use of Study Results. The Site shall maintain the security of Study subject data and shall obtain all authorizations or other necessary documentation from Study subjects to allow disclosures of Study subjects’ data to Sponsor and its agents and contractors, and, if this is a multi-site Study, with researchers at other Study sites, to the extent necessary for them to comply with this Agreement, the Privacy Regulations, and other Applicable Law, and for purposes related to the Study (including, without limitation, Study monitoring, analysis of Study data, and preparing applications and other reports to be submitted to regulatory authorities). The Institution and the Investigator agree to transfer to Sponsor only those data, including but not limited to clinical data regarding patients, which are made anonymous. This means that the data could be transferred by the Sponsor to any country in the world for processing including countries which do not have data protection laws as strict as those znamená, že údaje mohou být předávány Zadavatelem ke zpracování do jakékoli země na světě včetně zemí, které nemají tak přísné zákony o ochraně osobních údajů jako ty, které platí v Evropské unii (zejména Spojené státy americké). in force in the European Union (including, without limitation, the United States of America).

Appears in 1 contract

Sources: Sponsored Clinical Trial Agreement

Use of Study Results. The Site shall maintain the security of Study subject data and shall obtain all authorizations or other necessary documentation from Study subjects to allow disclosures of Study subjects’ data to Sponsor and its agents and contractors, and, if this is a multi-site Study, with researchers at other Study sites, to the extent necessary for them to comply with this Agreement, the Privacy Regulations, and other Applicable Law, and for purposes related to the Study (including, without limitation, Study monitoring, analysis of Study data, and preparing applications and other reports to be submitted to regulatory authorities). The Institution and the Investigator agree to transfer to Sponsor only those data, including but not limited to clinical data regarding patients, which are made anonymous. This means that the data could be transferred by the Sponsor to any country in the world for processing including countries which do not have data protection laws as strict as those pacientů, které budou anonymizovány. To znamená, že údaje mohou být předávány Zadavatelem ke zpracování do jakékoli země na světě včetně zemí, které nemají tak přísné zákony o ochraně osobních údajů jako ty, které platí v Evropské unii (zejména Spojené státy americké). do not have data protection laws as strict as those in force in the European Union (including, without limitation, the United States of America).

Appears in 1 contract

Sources: Sponsored Clinical Trial Agreement

Use of Study Results. The Site shall maintain the security of Study subject data and shall obtain all authorizations or other necessary documentation from Study subjects to allow disclosures of Study subjects’ data to Sponsor and its agents and contractors, and, if this is a multi-site Study, with researchers at other Study sites, to the extent necessary for them to comply with this Agreement, the Privacy Regulations, and other Applicable Law, and for purposes related to the Study (including, without limitation, Study monitoring, analysis of Study data, and preparing applications and other reports to be submitted to regulatory authorities). The Institution and the Investigator agree to transfer to Sponsor only those data, including but not limited to clinical data regarding patients, which are made anonymous. This means that the data could be transferred by the Sponsor to any country in the world for processing including countries which do not have data protection laws as strict as those Zkoušející souhlasí, že předají Zadavateli pouze ty údaje, zejména klinické údaje týkající se pacientů, které budou anonymizovány. To znamená, že údaje mohou být předávány Zadavatelem ke zpracování do jakékoli země na světě včetně zemí, které nemají tak přísné zákony o ochraně osobních údajů jako ty, které platí v Evropské unii (zejména Spojené státy americké). transferred by the Sponsor to any country in the world for processing including countries which do not have data protection laws as strict as those in force in the European Union (including, without limitation, the United States of America).

Appears in 1 contract

Sources: Sponsored Clinical Trial Agreement