Provisions of Data and Reports. The Institution shall provide to SPONSOR original case report forms (either in paper or electronic form if the Protocol calls for electronic data capture (EDC) ) (collectively, “CRFs”) completed for each Subject participating in the Study and such other reports as and when required by the applicable Protocol or Applicable Laws. The Institution shall provide the final CRFs required by the Study as set forth in the applicable SOW or such later date as SPONSOR may reasonably require.
Appears in 2 contracts
Sources: Master Clinical Study Agreement, Master Clinical Study Agreement
Provisions of Data and Reports. The Institution shall provide to SPONSOR original case report forms (either in paper or electronic form if the Protocol calls for electronic web-based data capture (EDCWBDC) system) (collectively, “CRFs”) completed for each Subject participating in the Study and such other reports as and when required by the applicable Protocol or Applicable Laws. The Institution shall provide the final CRFs required by the Study as set forth in the applicable SOW or such later date as SPONSOR may reasonably require.
Appears in 2 contracts
Sources: Master Clinical Study Agreement, Master Clinical Study Agreement
Provisions of Data and Reports. The Institution shall provide to SPONSOR original case report forms (either in paper or electronic form if the Protocol calls for electronic web=based data capture (EDCWBDC) system) (collectively, “CRFs”) completed for each Subject participating in the Study and such other reports as and when required by the applicable Protocol or Applicable Laws. The Institution shall provide the final CRFs required by the Study as set forth in the applicable SOW or such later date as SPONSOR may reasonably require.
Appears in 2 contracts
Sources: Master Clinical Study Agreement, Master Clinical Trial Agreement
Provisions of Data and Reports. The Institution shall provide to SPONSOR original case report forms (either in paper or electronic form if the Protocol calls for electronic data capture (EDC) ) (collectively, “CRFs”) completed for each Subject participating in the Study Trial and such other reports as and when required by the applicable Protocol or Applicable Laws. The Institution shall provide the final CRFs required by the Study Trial as set forth in the applicable SOW or such later date as SPONSOR may reasonably require.
Appears in 1 contract
Sources: Master Clinical Trial Agreement