Common use of SUB-STUDY FUNCTIONALITY Clause in Contracts

SUB-STUDY FUNCTIONALITY. The MSBase and MGBase Registry Websites provide a free logistic support tool for Investigator-initiated prospective ‘sub-studies’. Sub-studies typically contain a subset of the pseudonymised data pool pertaining to a particular research topic. Sub-studies currently active within the Registry include topics such as pregnancy and NIDs, demographics and NIDs, familial NIDs and drug safety/drug efficacy studies. These sub-studies may be national or international collaborations between member investigators with similar research interests. The sub-study module also enables the set-up and management of national, supranational, and regional registries. Centre PIs who initiate a sub-study on behalf of the Centre, become the leader of the sub-study. Once established, the sub-study can be joined by other Centres. The sub-studies leading PI can download encrypted datasets of the pseudonymised patient data records available within the sub-study. Note: by clicking ‘JOIN’ on a sub-study, each collaborating PI gives the leading PI permission to download, manage and use the shared subset of pseudonymised patient data for research. Collaborating PIs should read the study criteria carefully prior to joining any sub-study to ensure that they agree with the leading PI’s terms and conditions and ensure that their Centre Authority is agreeable with their Centre’s participation (as part of the PI delegated responsibilities).

SUB-STUDY FUNCTIONALITY. The MSBase and MGBase Registry Websites provide a free logistic support tool for Investigator-initiated prospective ‘sub-studies’. Sub-studies typically contain a subset of the pseudonymised data pool pertaining to a particular research topic. Sub-studies currently active within the Registry include topics such as pregnancy and NIDs, demographics and NIDs, familial NIDs and drug safety/drug efficacy studies. These sub-studies may be national or international collaborations between member investigators with similar research interests. The sub-study module also enables the set-up and management of national, supranational, and regional registries. Centre PIs who initiate a sub-study on behalf of the Centre, become the leader of the sub-study. Once established, the sub-study can be joined by other Centres. The sub-studies leading PI can download encrypted datasets of the pseudonymised patient data records available within the sub-study. Note: by clicking ‘JOIN’ on a sub-study, each collaborating PI gives the leading PI permission to download, manage and use the shared subset of pseudonymised patient data for research. Collaborating PIs PI’s should read the study criteria carefully prior to joining any sub-study to ensure that they agree with the leading PI’s terms and conditions and ensure that their Centre Authority is agreeable with their Centre’s participation (as part of the PI delegated responsibilities).

SUB-STUDY FUNCTIONALITY. The MSBase and MGBase Registry Websites provide Website provides a free logistic support tool for Investigator-Investigator- initiated prospective ‘sub-studies’. Sub-studies typically contain a subset of the pseudonymised data pool pertaining to a particular research topic. Sub-studies currently active within the Registry include topics such as pregnancy and NIDs, demographics and NIDs, familial NIDs and drug safety/drug efficacy studies. These sub-studies may be national or international collaborations between member investigators with similar research interests. The sub-study module also enables the set-up and management of national, supranational, and regional registries. Centre PIs who initiate a sub-study on behalf of the Centre, become the leader of the sub-study. Once established, the sub-study can be joined by other Centres. The sub-studies leading PI can download encrypted datasets of the pseudonymised patient data records available within the sub-study. Note: by clicking ‘JOIN’ on a sub-study, each collaborating PI gives the leading PI permission to download, manage and use the shared subset of pseudonymised patient data for research. Collaborating PIs PI’s should read the study criteria carefully prior to joining any sub-study to ensure that they agree with the leading PI’s terms and conditions and ensure that their Centre Authority is agreeable with their Centre’s participation (as part of the PI delegated responsibilities).