Common use of Retention of Data Clause in Contracts

Retention of Data. The Institution and the Investigator undertake to keep and store all Trial-related documents including, without limitation, the Subjects’ informed consent forms regarding the Study, CRFs, original data and ISF, at least for a minimum period of fifteen (15) years from the completion of the Trial, in a manner required by the Applicable Laws and Regulations and securing protection of the Trial Subjects’ personal data according to applicable personal data protection laws, namely the Data Protection Law.

Appears in 4 contracts

Samples: Clinical Trial Agreement, Clinical Trial Agreement, Clinical Trial Agreement

AutoNDA by SimpleDocs

Retention of Data. The Institution and the Investigator undertake undertakes to keep and store all Trial-related documents including, without limitation, the Subjects’ informed consent forms regarding the StudyTrial, CRFs, original data and ISF, at least for a minimum period of fifteen (15) years from the completion of the Trial, in a manner required by the Applicable Laws and Regulations and securing protection of the Trial Subjects’ personal data according to applicable personal data protection laws, namely the Data údajů, zejména Právními předpisy na ochranu osobních údajů. Protection Law.

Appears in 1 contract

Samples: Clinical Trial Agreement

Retention of Data. The Institution and the Investigator undertake undertakes to keep and store all Trial-related documents including, without limitation, the Subjects’ informed consent forms regarding the StudyTrial, CRFs, original data and ISF, at least for a minimum period of fifteen (15) years from the completion of the Trial, in a manner required by the Applicable Laws and Regulations and securing protection of the Trial Subjects’ personal data according to applicable personal data protection laws, namely the Data Protection Law.

Appears in 1 contract

Samples: Clinical Trial Agreement

AutoNDA by SimpleDocs

Retention of Data. The Institution and the Investigator undertake undertakes to keep and store all Trial-related documents including, without limitation, the Subjects’ informed consent forms regarding the StudyTrial, CRFs, original data and ISF, at least for a minimum period of fifteen (15) years from the completion of the Trial, in a manner required by the Applicable Laws and Regulations and securing protection of the Trial Subjects’ personal data according to applicable personal data protection laws, namely the Data Protection Law.

Appears in 1 contract

Samples: Clinical Trial Agreement

Draft better contracts in just 5 minutes Get the weekly Law Insider newsletter packed with expert videos, webinars, ebooks, and more!