SUB-STUDY FUNCTIONALITY Sample Clauses

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).
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Related to SUB-STUDY FUNCTIONALITY

  • Additional Functionality Microsoft may provide additional functionality for the software. Other license terms and fees may apply.

  • Future Functionality You agree that Your purchases are not contingent on the delivery of any future functionality or features, or dependent on any oral or written public comments made by Us regarding future functionality or features.

  • Study Population ‌ Infants who underwent creation of an enterostomy receiving postoperative care and awaiting enterostomy closure: to be assessed for eligibility: n = 201 to be assigned to the study: n = 106 to be analysed: n = 106 Duration of intervention per patient of the intervention group: 6 weeks between enterostomy creation and enterostomy closure Follow-up per patient: 3 months, 6 months and 12 months post enterostomy closure, following enterostomy closure (12-month follow-up only applicable for patients that are recruited early enough to complete this follow-up within the 48 month of overall study duration).

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  • Screening 3.13.1 Refuse containers located outside the building shall be fully screened from adjacent properties and from streets by means of opaque fencing or masonry walls with suitable landscaping.

  • Cutting, Patching, and Fitting The Contractor shall do all cutting, patching, and fitting of the Work that may be required to make its several parts come together properly and fit.

  • Joint Network Implementation and Grooming Process Upon request of either Party, the Parties shall jointly develop an implementation and grooming process (the “Joint Grooming Process” or “Joint Process”) which may define and detail, inter alia:

  • Interoperability To the extent required by applicable law, Cisco shall provide You with the interface information needed to achieve interoperability between the Software and another independently created program. Cisco will provide this interface information at Your written request after you pay Cisco’s licensing fees (if any). You will keep this information in strict confidence and strictly follow any applicable terms and conditions upon which Cisco makes such information available.

  • Study An application for leave of absence for professional study must be supported by a written statement indicating what study or research is to be undertaken, or, if applicable, what subjects are to be studied and at what institutions.

  • Protocol No action to coerce or censor or penalize any negotiation participant shall be made or implied by any other member as a result of participation in the negotiation process.

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