Without limiting the generality. of Section 11.1, Investigator hereby represent and warrant that they shall utilize one or more lawful bases under Data Protection Law legitimizing, and comply with the requirement to notify study Subjects through Informed Consent Form- General Data Protection, provided by SPONSOR/ CRO. Investigator’s and Study Personnel of the Personal Data Processing so that such study Subjects’, Study Personnel’s and Investigator’s Personal Data can be Processed by (including transferred to) SPONSOR its designee or any of its Affiliates and regulatory authorities in each case within or outside the country where such data originates.
Appears in 1 contract
Sources: Clinical Site Agreement
Without limiting the generality. of Section 11.1, Institution and/or Investigator hereby represent and warrant that they shall utilize one or more lawful bases under Data Protection Law legitimizing, and comply with the requirement to notify study Subjects through Informed Consent Form- General Data ProtectionSubjects, provided by SPONSOR/ CRO. Investigator’s and Study Personnel of the Personal Data Processing so that such study Subjects’, Study Personnel’s and Investigator’s Personal Data can be Processed by (including transferred to) SPONSOR its designee or any of its Affiliates and regulatory authorities in each case within or outside the country where such data originates.
Appears in 1 contract
Sources: Clinical Site Agreement
Without limiting the generality. of Section 11.1, Investigator hereby represent and warrant that they shall utilize one or more lawful bases under Applicable Law legitimizing the Personal Data Protection Law legitimizingProcessing, and comply with the requirement to notify study Subjects through Informed Consent Form- General Data ProtectionSubjects, provided by SPONSOR/ CRO. Investigator’s and Study Personnel of the Personal Data Processing Processing, so that such study Study Subjects’, Study Personnel’s and Investigator’s Personal Data can be Processed by (including transferred to) CRO, any of its Affiliates, and SPONSOR its designee or any of its Affiliates and regulatory authorities in each case within or outside the country where such data originates.
Appears in 1 contract
Sources: Clinical Trial Agreement