Study Subject Personal Data. The Investigator shall obtain Study Subject written consent for the collection and use of Study Subject personal data for Study purposes, including the disclosure, transfer and processing of data collected in accordance with the Protocol, in compliance with applicable data protection provisions.
Appears in 17 contracts
Samples: Clinical Trial Agreement, Clinical Trial Agreement, Clinical Trial Agreement
Study Subject Personal Data. The Investigator shall obtain Study Subject written consent for the collection and use of Study Subject personal data Personal Data for Study purposes, including the disclosure, transfer and processing of data collected in accordance with the Protocol, in compliance with applicable data protection provisions.
Appears in 2 contracts
Study Subject Personal Data. The Investigator shall obtain Study Subject written consent for the collection and use of Study Subject personal data for Study purposes, including the disclosure, transfer and processing of data collected in accordance with the Protocol, in compliance with applicable data protection provisionspředpisy a nařízeními a bude oznamovat výsledky Studie veřejně tehdy a v rozsahu uloženém příslušnými právními předpisy a nařízeními.
Appears in 1 contract
Samples: Clinical Trial Agreement
Study Subject Personal Data. The Investigator shall obtain Study Subject written informed consent for the collection and use of Study Subject personal data for Study purposes, including the disclosure, transfer and processing of data collected in accordance with the Protocol, in in
6.1 Osobní údaje
6.2 Osobní údaje Subjektu studie Zkoušející zajistí získání písemného informovaného souhlasu Subjektu studie pro účely k získání a použití osobních údajů Subjektu studie pro účely související se Studií, a to včetně odhalení, převodu a zpracování osobních údajů získaných dle Protokolu, a compliance with applicable data protection provisions.
Appears in 1 contract
Samples: Clinical Trial Agreement
Study Subject Personal Data. The Investigator shall obtain Study Subject written consent for the collection and use of Study Subject personal data Personal Data for Study purposes, including the disclosure, transfer and processing of data collected in accordance with the Protocol, in compliance with applicable data protection provisions. Zkoušející zajistí získání písemného souhlasu Subjektu studie pro účely k získání a použití osobních údajů Subjektu studie pro účely související se Studií, a to včetně odhalení, převodu a zpracování osobních údajů získaných dle Protokolu, a dále v souladu s příslušnými předpisy na poli ochrany dat.
Appears in 1 contract
Samples: Clinical Trial Agreement
Study Subject Personal Data. The Investigator shall obtain Study Subject subject written consent for the collection and use of Study Subject subject personal data for Study purposes, including the disclosure, transfer and processing of data collected in accordance with the Protocol, in compliance with applicable data protection provisions.
Appears in 1 contract
Samples: Clinical Trial Agreement
Study Subject Personal Data. The Investigator shall obtain Study Subject written consent for the collection and use of Study Subject personal data for Study purposes, including the disclosure, transfer and processing of data collected in accordance with the Protocol, in compliance with applicable data protection provisions, namely of Act No. 101/2000 Coll., on Personal Data Protection, as amended.
Appears in 1 contract
Samples: Clinical Trial Agreement
Study Subject Personal Data. The Investigator shall obtain Study Subject written consent for the collection and use of Study Subject personal data for Study purposes, including the disclosure, transfer and processing of data collected in accordance with the Protocol, in compliance with applicable data protection provisions.provisions and the Data Processing Agreement in Attachment B. 6.3
Appears in 1 contract
Samples: Clinical Trial Agreement