Common use of Rights of Data Subjects Participating in the Clinical Trial Clause in Contracts

Rights of Data Subjects Participating in the Clinical Trial. Center and Sponsor agree that, as between them, Center is best able to manage data protection requests from trial subjects and will will respond to trial subjects’ requests in accordance with applicable law. Center will promptly notify Sponsor at . of any withdrawal of any consent to data processing provided by a trial subject.

Rights of Data Subjects Participating in the Clinical Trial. Center and Sponsor agree that, as between them, Center is best able to manage data protection requests from trial subjects and will will respond to trial subjects’ requests in accordance with applicable law. Center will promptly notify Sponsor at . XXX of any withdrawal of any consent to data processing provided by a trial subject.. 10.6.4

Rights of Data Subjects Participating in the Clinical Trial. Center and Sponsor agree that, as between them, Center is best able to manage data protection requests from trial subjects and will will respond to trial subjects’ requests in accordance with applicable law. Center will promptly notify Sponsor at . XXX of any withdrawal of any consent to data processing provided by a trial subject.. 10.6.5

Rights of Data Subjects Participating in the Clinical Trial. Center and Sponsor agree that, as between them, Center is best able to manage data protection requests from trial subjects and will will respond to trial subjects’ requests in accordance with applicable law. Center will promptly notify Sponsor at . of any withdrawal of any consent to data processing provided by a trial subject.. 1.5

Rights of Data Subjects Participating in the Clinical Trial. Center and Sponsor agree that, as between them, Center is best able to manage data protection requests from trial subjects and will will respond to trial subjects’ requests in accordance with applicable law. Center will promptly notify Sponsor at . .........................of any withdrawal of any consent to data processing provided by a trial subject.. 10.6.4

Rights of Data Subjects Participating in the Clinical Trial. Center and Sponsor agree that, as between them, Center is best able to manage data protection requests from trial subjects and will will respond to trial subjects’ requests in accordance with applicable law. Center will promptly notify Sponsor at . of any withdrawal of any consent to data processing provided by a trial subject.. 10.6.5

Rights of Data Subjects Participating in the Clinical Trial. Center and Sponsor agree that, as between them, Center is best able to manage data protection requests from trial subjects and will will respond to trial subjects’ requests in accordance with applicable law. Center will promptly notify Sponsor at . xxx of any withdrawal of any consent to data processing provided by a trial subject.. 10.6.4

Rights of Data Subjects Participating in the Clinical Trial. Center and Sponsor agree that, as between them, Center is best able to manage data protection requests from trial subjects and will will respond to trial subjects’ requests in accordance with applicable law. Center will promptly notify Sponsor at . XXX of any withdrawal of any consent to data processing provided by a trial subject.. každom stiahnutí akéhokoľvek súhlasu so spracovaním údajov subjektu skúšania. 10.5.5

Rights of Data Subjects Participating in the Clinical Trial. Center and Sponsor agree that, as between them, Center is best able to manage data protection requests from trial subjects and will will respond to trial subjects’ requests in accordance with applicable law. Center will promptly oromotlv notify Sponsor at . _ of any withdrawal of any consent to data processing provided by a trial subject.