Common use of Study Subject Personal Data Clause in 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 provisions. 6.3

Appears in 13 contracts

Samples: Trial Agreement, Clinical Trial Agreement, Clinical Trial Agreement Smlouva O Klinickém

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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. 6.3.

Appears in 2 contracts

Samples: Trial Agreement, Clinical Trial Agreement Zmluva O Klinickom Skúšaní

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. 6.3.

Appears in 2 contracts

Samples: Clinical Trial Agreement, Trial Agreement Smlouva O Klinickém

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 provisionsTento Článek 5 “Práva na zveřejnění” zůstane v platnosti i v případě ukončení platnosti či při vypršení platnosti této Smlouvy. 6.36

Appears in 1 contract

Samples: Trial Agreement Smlouva O Klinickém

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. 6.3data

Appears in 1 contract

Samples: Entire 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. 6.310.2 Osobní údaje subjektů ve Studii. Zkoušející získá od každého subjektu ve Studii písemný informovaný souhlas se shromažďováním a používáním osobních údajů daného subjektu pro účely Studie, včetně sdělování, předávání a zpracovávání shromážděných údajů v souladu s Protokolem a s platnými právními předpisy o ochraně osobních údajů.

Appears in 1 contract

Samples: smlouvy.gov.cz

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 compliance with applicable data protection provisions. 6.3in

Appears in 1 contract

Samples: Clinical Trial Agreement

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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. 6.3

Appears in 1 contract

Samples: 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. 6.3předpisy a nařízeními a bude oznamovat výsledky Studie veřejně tehdy a v rozsahu uloženém příslušnými právními předpisy a nařízeními.

Appears in 1 contract

Samples: 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

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