Data Collection and Data Management. 3.1.3.1 CRF. Opthea will be solely responsible for preparing the form of Case Report Form for each of the Product Clinical Trials in accordance with the applicable Protocol.
Appears in 1 contract
Data Collection and Data Management. 3.1.3.1 CRF. Opthea will be solely responsible for preparing the form of Case Report Form for each of the Product Clinical Trials in accordance with the applicable Protocol.
Appears in 1 contract