Study Methodology, Scope and Limitations Sample Clauses

Study Methodology, Scope and Limitations. The GSs included in this project do not cause any loss of productive and other assets (including land), income and livelihoods, and thus requires lesser consideration in this resettlement and compensation plan. In case of the five transmission lines, the work is presently at a preliminary level. The technical specifications of the lines have been finalised, and preliminary identification of the line routing has been completed with map-based assessments followed by field visits by CEB engineering staff and Environmental Officers. This study extensively draws upon the experience of CEB staff who have been working on the planning and design phases of the GSs, and the information collected during site visits. In case of transmission lines, the study draws on the experience of CEB design engineers about the route, and the information obtained from other experts in areas such as biodiversity impacts along the proposed corridor. This study reflects the information available from different sources stated above at the time of writing (November 2007). A specific limitation exists with regard to the finalisation of corridor for the five transmission lines under this project, which will be done at the next phase of project development. While the selected alternative for each line corridor is acceptable to CEB, specific conditions stipulated during the environmental approval process and the subsequent process of addressing grievances of affected persons, may require minor 4 Handbook on Resettlement, A Guide to Good Practice, Asian Development Bank, 1998. Also see ADB Policy on Involuntary Resettlement, Aug 1995. 5 Operational Manual Bank Policies: Involuntary Resettlement, 25 Sep 2006 deviation from the proposed routing, and these deviations can only be confirmed after the detailed route surveys have been completed, notices are issued in accordance with the Electricity Act, and objections are resolved by the relevant DSs. The updated resettlement plan will be submitted to ADB, after the detailed surveys have been completed. 3 MINIMISATION OF IMPACTS AND MITIGATORY MEASURES
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Related to Study Methodology, Scope and Limitations

  • Testing Procedure Limitations The Asset Representations Reviewer will only be required to perform the testing procedures listed under “Tests” in Schedule A, and will have no obligation to perform additional procedures on any Subject Lease or to provide any information other than a Review Report indicating for each Subject Lease whether there was a Test Pass or a Test Fail for each Test, or whether the Subject Lease was a Test Complete and the related reason. However, the Asset Representations Reviewer may provide additional information about any Subject Lease that it determines in good faith to be material to the Review.

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  • Tests and Preclinical and Clinical Trials The preclinical studies and clinical trials conducted by or, to the Company’s knowledge, on behalf of the Company, that are described in the Registration Statement, the Pricing Disclosure Package and the Prospectus, as applicable, and are intended to be submitted to the U.S. Food and Drug Administration (the “FDA”) or other comparable government entities, 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, current Good Clinical Practices and Good Laboratory Practices and any applicable rules and regulations of the jurisdiction in which such trials and studies are being conducted; the descriptions of the results of such studies and trials contained in the Registration Statement, the Pricing Disclosure Package and the Prospectus are, to the Company’s knowledge, accurate and complete in all material respects and fairly present the data derived from such studies and trials; except to the extent disclosed in the Registration Statement, the Pricing Disclosure Package and the Prospectus, the Company is not aware of any studies or trials, the results of which the Company believes reasonably call into question the study or trial results described or referred to in the Registration Statement, the Pricing Disclosure Package and the Prospectus when viewed in the context in which such results are described and the clinical stage of development; and, except to the extent disclosed in the Registration Statement, the Pricing Disclosure Package or the Prospectus, the Company has not received any written notices or written correspondence from the FDA or any governmental entity requiring the termination or suspension of any preclinical studies 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.

  • Research Use Reporting To assure adherence to NIH GDS Policy, the PI agrees to provide annual Progress Updates as part of the annual Project Renewal or Project Close-out processes, prior to the expiration of the one (1) year data access period. The PI who is seeking Renewal or Close-out of a project agree to complete the appropriate online forms and provide specific information such as how the data have been used, including publications or presentations that resulted from the use of the requested dataset(s), a summary of any plans for future research use (if the PI is seeking renewal), any violations of the terms of access described within this Agreement and the implemented remediation, and information on any downstream intellectual property generated from the data. The PI also may include general comments regarding suggestions for improving the data access process in general. Information provided in the progress updates helps NIH evaluate program activities and may be considered by the NIH GDS governance committees as part of NIH’s effort to provide ongoing stewardship of data sharing activities subject to the NIH GDS Policy.

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