Rights of Data Subjects Participating in the Clinical Trial Clause Samples
The 'Rights of Data Subjects Participating in the Clinical Trial' clause defines the protections and entitlements granted to individuals whose personal data is collected during a clinical study. It typically outlines participants' rights to access, correct, or request deletion of their personal information, and may specify how consent is obtained and how data privacy is maintained throughout the trial. This clause ensures compliance with data protection laws and safeguards participants' privacy, addressing concerns about misuse or unauthorized disclosure of sensitive information.
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.
Rights of Data Subjects Participating in the Clinical Trial. Parties - Center and Sponsor agree that, as Centrum najlepšie schopné riadiť žiadosti týkajúce sa ochrany osobných údajov od subjektov skúšania a bude odpovedať na žiadosti subjektov skúšania v súlade s platnými právnymi predpismi. Centrum bezodkladne informuje Zadávateľa na adrese XXX o každom stiahnutí akéhokoľvek súhlasu so spracovaním údajov subjektu skúšania. Adresa Centra pre účely akýchkoľvek dotazov, ktoré sa vyskytnú, je ▇▇▇▇▇▇▇▇▇▇▇▇▇▇▇@▇▇▇▇▇▇▇▇▇.▇▇ between them, Center is best able to manage personal data protection requests from trial subjects and 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. The Center’s contact email address for any questions arising is: ▇▇▇▇▇▇▇▇▇▇▇▇▇▇▇@▇▇▇▇▇▇▇▇▇.▇▇.