GOVERNANCE OF SUB-STUDIES. All collaboration in sub-studies is voluntary and joining a sub-study implies a mutual agreement between the Sub-Study Leader and each other participating Centre to share data for the purpose of the sub-studies aim(s) and objective(s). Many sub-studies can be conducted using the dataset available in the Registry as outlined in the MSBase/MGBase Registry Observational Study Protocol. Some sub-studies also require the collection of additional data fields or require interventions that are not covered by the Study Protocol. For these collaborative sub-studies, Centres and their authorised PIs must ensure that they fulfil any additional regulatory and legal requirements, including, for example, obtainment of additional ethical approvals and/or updates to the Patient Informed Consent Form.
Appears in 3 contracts
Samples: Registry Participation Agreement, Registry Participation Agreement, Registry Participation Agreement
GOVERNANCE OF SUB-STUDIES. All collaboration in sub-studies is voluntary and joining a sub-study implies a mutual agreement between the Sub-Study Leader and each other participating Centre to share data for the purpose of the sub-studies aim(s) and objective(s). Many sub-studies can be conducted using the dataset available in the Registry (the MSBase MDS Data Dictionary documents a comprehensive list of these fields) as outlined in the MSBase/MGBase MSBase Registry Observational Study Protocol. Some sub-studies also require the collection of additional data fields or require interventions that are not covered by the Study Protocol. For these collaborative sub-studies, Centres and their authorised PIs PI’s must ensure that they fulfil any additional regulatory and regulatory, legal requirements, including, for . For example, obtainment of additional ethical approvals and/or updates to the Patient Informed Consent Form.
Appears in 1 contract
GOVERNANCE OF SUB-STUDIES. All collaboration in sub-studies is voluntary and joining a sub-study implies a mutual agreement between the Sub-Study Leader and each other participating Centre to share data for the purpose of the sub-studies aim(s) and objective(s). Many sub-studies can be conducted using the dataset available in the Registry (the MSBase MDS Data Dictionary documents a comprehensive list of these fields) as outlined in the MSBase/MGBase Registry Observational Study Protocol. Some sub-studies also require the collection of additional data fields or require interventions that are not covered by the Study Protocol. For these collaborative sub-studies, Centres and their authorised PIs PI’s must ensure that they fulfil any additional regulatory and regulatory, legal requirements, including, for . For example, obtainment of additional ethical approvals and/or updates to the Patient Informed Consent Form.
Appears in 1 contract
Samples: Registry Participation Agreement
GOVERNANCE OF SUB-STUDIES. All collaboration in sub-studies is voluntary and joining a sub-study implies a mutual agreement between the Sub-Study Leader and each other participating Centre to share data for the purpose of the sub-studies aim(s) and objective(s). Many sub-studies can be conducted using the dataset available in the Registry as outlined in the MSBase/MGBase Registry Observational Study Protocol. Some sub-studies also require the collection of additional data fields or require interventions that are not covered by the Study Protocol. For these collaborative sub-studies, Centres and their authorised PIs must ensure that they fulfil any additional regulatory and legal requirements, including, for including,.for example, obtainment of additional ethical approvals and/or updates to the Patient Informed Consent Form.
Appears in 1 contract
Samples: Registry Participation Agreement