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 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. Biogen Idec agrees to reimburse the Institution for costs related to document archiving as noted in payment tables of Schedule A – Payments.

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 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. Biogen Idec agrees to reimburse the Institution for costs related to document archiving as noted in payment tables of Schedule A – Payments.

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 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. Biogen Idec agrees to reimburse the Institution for costs related to document archiving as noted in payment tables of Schedule A – Payments.. (e)

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 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. Biogen Idec agrees to reimburse the Institution for costs related to document archiving as noted in payment tables of Schedule A – PaymentsBudget & Payment Schedule.