Common use of Data and Document Sharing Clause in Contracts

Data and Document Sharing. Institution and Investigator acknowledge that, Sponsor may, in accordance with the joint ‘Principles for Responsible Clinical Trial Data Sharing’ by EFPIA and PhRMA (found at: xxx.xxxxx.xx or xxx.xxxxx.xxx), share the clinical study report, related clinical documents, and patient-level clinical study data with third party requestors (more information to be found at xxxx://xxxxxx.xxxxxxxxxx- xxxxxxxxx.xxx/xxxxxxxxxxxx policy.html) .

Appears in 1 contract

Samples: Clinical Trial Agreement

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Data and Document Sharing. Institution Provider and Investigator acknowledge that, Sponsor may, in accordance with the joint ‘Principles for Responsible Clinical Trial Data Sharing’ by EFPIA and PhRMA (found at: xxx.xxxxx.xx or xxx.xxxxx.xxx), share the clinical study report, related clinical documents, and patient-level clinical study data with third party requestors (more information to be found at xxxx://xxxxxx.xxxxxxxxxx- xxxxxxxxx.xxx/xxxxxxxxxxxx policy.html) xxxxxxxxx.xxx/xxxxxxxxxxxx_xxxxxx.xx ml). výsledky Klinického hodnocení.

Appears in 1 contract

Samples: Clinical Trial Agreement

Data and Document Sharing. Institution and Investigator acknowledge that, Sponsor may, in accordance with the joint ‘Principles for Responsible Clinical Trial Data Sharing’ by EFPIA and PhRMA (found at: xxx.xxxxx.xx or xxx.xxxxx.xxx), share the clinical study report, related clinical documents, and patient-level clinical study data with third party requestors (more information to be found at xxxx://xxxxxx.xxxxxxxxxx- xxxxxxxxx.xxx/xxxxxxxxxxxx policy.html) .xxxx://xxxxxx.xxxxxxxxxx-xxxxxxxxx.xxx/ transparency_policy.html). 9.3

Appears in 1 contract

Samples: Master Clinical Trial Agreement

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Data and Document Sharing. Institution and Investigator acknowledge that, Sponsor may, in accordance with the joint ‘Principles for Responsible Clinical Trial Data Sharing’ by EFPIA and PhRMA (found at: xxx.xxxxx.xx or xxx.xxxxx.xxx), share the clinical study report, related clinical documents, and patient-level clinical study data with third party requestors (more information to be found at xxxx://xxxxxx.xxxxxxxxxx- xxxxxxxxx.xxx/xxxxxxxxxxxx policy.html) xxxxxxxxx.xxx/xxxxxxxxxxxx_xxxxxx.xxx l).

Appears in 1 contract

Samples: Clinical Trial Agreement

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