Study Participants Personal Data. Role and qualification of the Parties SPONSOR is subject to the rights and obligations as “controller” set forth under the GDPR in relation to the processing of Personal Data for the purpose of conducting the Study in accordance with the Protocol, the informed consent form and this Agreement. In that respect SPONSOR shall be considered as controller of all Personal Data processed for Study purposes. INSTITUTION is subject to the rights and obligations as “processor” set forth under the GDPR in relation to the processing of Personal Data for the purpose of conducting the Study in accordance with the Protocol, the informed consent form and this Agreement. Pursuant to Article 28.3 GDPR SPONSOR and INSTITUTION have concluded a data processing agreement attached in SCHEDULE F. INSTITUTION is also subject to the rights and obligations as a separate “controller” set forth under the GDPR in relation to the processing of Personal Data of its patients for purposes other than conducting the Study. In particular, INSTITUTION remains controller of the data contained in its patients’ medical records for the purposes of providing medical care to its patients and for academic research purposes.
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Samples: Draft Agreement, Draft Agreement, Draft Agreement
Study Participants Personal Data. Role and qualification of the Parties SPONSOR is subject to the rights and obligations as “controller” set forth under the GDPR in relation to the processing of Personal Data for the purpose of conducting the Study in accordance with the Protocol, the informed consent form and this Agreement. In that respect SPONSOR shall be considered as controller of all Personal Data processed for Study purposes. INSTITUTION is subject to the rights and obligations as “processor” set forth under the GDPR in relation to the processing of Personal Data for the purpose of conducting the Study in accordance with the Protocol, the informed consent form and this Agreement. Pursuant to Article 28.3 GDPR SPONSOR and INSTITUTION have concluded a data processing agreement attached in SCHEDULE F. . INSTITUTION is also subject to the rights and obligations as a separate “controller” set forth under the GDPR in relation to the processing of Personal Data of its patients for purposes other than conducting the Study. In particular, INSTITUTION remains controller of the data contained in its patients’ medical records for the purposes of providing medical care to its patients and for academic research purposes.
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Samples: gbiomed.kuleuven.be