Trial Subject Personal Data. The Principal Investigator shall obtain Trial Subject written consent for the collection and use of Trial Subject personal data for Trial purposes as a condition of the Trial Subject participating in the Trial, including the disclosure, transfer and processing of data collected in accordance with the Protocol, in compliance with applicable data protection provisions.
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Trial Subject Personal Data. The Principal Investigator shall obtain Trial Subject written consent for the collection and use of Trial Subject personal data for Trial purposes as a condition of the Trial Subject participating in the Trialpurposes, including the disclosure, transfer transfer, and processing of data collected in accordance with wit h the Protocol, in compliance with wit h applicable data protection provisions.
Appears in 1 contract
Samples: Clinical Trial Agreement
Trial Subject Personal Data. The Principal Investigator shall obtain Trial Subject written consent for the collection and use of Trial Subject personal data for Trial purposes as a condition of the Trial Subject participating in the Trialpurposes, including the disclosure, transfer transfer, and processing of data collected in accordance with the Protocol, in compliance with applicable data protection provisions.. 13.3
Appears in 1 contract
Samples: Clinical Trial Agreement
