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_xxxxxx.xxx l).

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_xxxxxx.xxx lxxxxxxxxx.xxx/xxxxxxxxxxxx_xxxxxx.xx ml). výsledky Klinického hodnocení.

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_xxxxxx.xxx l)requestors.

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_xxxxxx.xxx lxxxx://xxxxxx.xxxxxxxxxx-xxxxxxxxx.xxx/ transparency_policy.html).

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_xxxxxx.xxx lxxxxxxxxx.xxx/xxxxxxxxxxxx xxxxxx.xx ml).

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_xxxxxx.xxx l)xxxxxxxxx.xxx/xxxxxxxxxxxx policy.html) .