DATA ANALYSIS AND CONCLUSION 40 Sample Clauses

DATA ANALYSIS AND CONCLUSION 40. The European Commission support for the production of this project does not constitute an endorsement of the contents which reflects the views only of the authors, and the Commission cannot be held responsible for any use which may be made of the information contained therein 4.1 Mapping of existing e-Governance courses with e-Governance research areas identified in task 1 40 4.2 Training Needs 40 4.3 Conclusion 42 The European Commission support for the production of this project does not constitute an endorsement of the contents which reflects the views only of the authors, and the Commission cannot be held responsible for any use which may be made of the information contained therein Figure1: Task 2 phases – process-tool design, data collection, and data analysis 10 Figure2: Survey design process 13 Figure3: 5-point Likert scale used in the survey questions 13 Figure 1: Training Programs (U: Undergraduate, P: Postgraduate) 15 Figure 2: e-Governance training programs categorized based on the certificate they award 16 Figure 3: Word cloud of the program names 16 Figure 4: Programs allocated in countries 17 Figure 5: Programs allocation based on Xxxxx’x taxonomy categories 18 Figure 6: Distribution of Program Specialisation Areas 20 Figure 7: Distribution of Program Degree Titles 20 Figure 8: Institution Types 21 Figure 9: Departments providing the training programs 21 Figure 10: Teaching Methods 23 Figure 11: Sex of the respondents 33 Figure 12: Key roles in e-Governance 34 Figure 13: Required skills in e-Governance 34 Figure 14: Lacking knowledge in e-Governance 37 Figure 15: Main objective of a master program in e-Governance 37 Figure 16: Significance of courses in an e-Governance program 38 Figure 17: Top selected e-Governance modules 39 Figure 1: e-Governance research areas appeared in titles and descriptions of identified courses 40 Figure 2: e-Governance courses (derived from the survey) mapped with existing courses 41 Figure 3: e-Governance modules (derived from the survey) related with existing courses 42 The European Commission support for the production of this project does not constitute an endorsement of the contents which reflects the views only of the authors, and the Commission cannot be held responsible for any use which may be made of the information contained therein Table 1: Sex of the respondents by age 33 Table 2: Education and occupation of the respondents 33 Table 3: Cross analysis between key roles and key skills in e-Governance (s...

Related to DATA ANALYSIS AND CONCLUSION 40

  • Investment Analysis and Implementation In carrying out its obligations under Section 1 hereof, the Advisor shall: (a) supervise all aspects of the operations of the Funds; (b) obtain and evaluate pertinent information about significant developments and economic, statistical and financial data, domestic, foreign or otherwise, whether affecting the economy generally or the Funds, and whether concerning the individual issuers whose securities are included in the assets of the Funds or the activities in which such issuers engage, or with respect to securities which the Advisor considers desirable for inclusion in the Funds' assets; (c) determine which issuers and securities shall be represented in the Funds' investment portfolios and regularly report thereon to the Board of Trustees; (d) formulate and implement continuing programs for the purchases and sales of the securities of such issuers and regularly report thereon to the Board of Trustees; and (e) take, on behalf of the Trust and the Funds, all actions which appear to the Trust and the Funds necessary to carry into effect such purchase and sale programs and supervisory functions as aforesaid, including but not limited to the placing of orders for the purchase and sale of securities for the Funds.

  • Statistical Sampling Documentation a. A copy of the printout of the random numbers generated by the “Random Numbers” function of the statistical sampling software used by the IRO.‌ b. A description or identification of the statistical sampling software package used by the IRO.‌

  • Risk Analysis The Custodian will provide the Fund with a Risk Analysis with respect to Securities Depositories operating in the countries listed in Appendix B. If the Custodian is unable to provide a Risk Analysis with respect to a particular Securities Depository, it will notify the Fund. If a new Securities Depository commences operation in one of the Appendix B countries, the Custodian will provide the Fund with a Risk Analysis in a reasonably practicable time after such Securities Depository becomes operational. If a new country is added to Appendix B, the Custodian will provide the Fund with a Risk Analysis with respect to each Securities Depository in that country within a reasonably practicable time after the addition of the country to Appendix B.

  • Quantitative Analysis Quantitative analysts develop and apply financial models designed to enable equity portfolio managers and fundamental analysts to screen potential and current investments, assess relative risk and enhance performance relative to benchmarks and peers. To the extent that such services are to be provided with respect to any Account which is a registered investment company, Categories 3, 4 and 5 above shall be treated as “investment advisory services” for purposes of Section 5(b) of the Agreement.”

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  • Tests and Preclinical and Clinical Trials The studies, tests and preclinical and clinical trials conducted by or, to the Company’s knowledge, on behalf of the Company were and, if still ongoing, are being conducted in all material respects in accordance with experimental protocols, procedures and controls pursuant to accepted professional scientific standards and all Authorizations and Applicable Laws, including, without limitation, the Federal Food, Drug and Cosmetic Act and the rules and regulations promulgated thereunder (collectively, “FFDCA”); the descriptions of the results of such studies, tests and trials contained in the Registration Statement, the General Disclosure Package and the Prospectus are, to the Company’s knowledge, accurate in all material respects and fairly present the data derived from such studies, tests and trials; except to the extent disclosed in the Registration Statement, the General Disclosure Package and the Prospectus, the Company is not aware of any studies, tests or trials, the results of which the Company believes reasonably call into question the study, test, or trial results described or referred to in the Registration Statement, the General Disclosure Package and the Prospectus when viewed in the context in which such results are described and the clinical state of development; and, except to the extent disclosed in the Registration Statement, the General Disclosure Package or the Prospectus, neither the Company nor any Subsidiary has received any notices or correspondence from the FDA or any Governmental Entity requiring the termination or suspension of any studies, tests or preclinical or clinical trials conducted by or on behalf of the Company, other than ordinary course communications with respect to modifications in connection with the design and implementation of such trials, copies of which communications have been made available to you.

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