SURVEYS AND STUDIES Sample Clauses

SURVEYS AND STUDIES. A. Geotechnical Engineering Study
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SURVEYS AND STUDIES. Seller shall promptly provide Purchaser with information and documentation (to the extent same is reasonably available) requested by Purchaser to facilitate its evaluation of the Property. During the Inspection Period Purchaser shall be permitted to enter the Property and to inspect and evaluate the Property, to conduct studies thereon, and to interview tenants, if any. If Purchaser determines for any reason that the Property is not suitable for Purchaser's purposes, Purchaser may terminate this Contract by giving written notice of same to Seller prior to 5:00 p.m. on the last day of the Inspection Period. Upon termination of this Contract pursuant hereto, Escrow Agent shall refund the Xxxxxxx Money to Purchaser. To the extent permitted by law, Purchaser shall hold Seller harmless from any damage caused by Purchaser, its agents or contractors, in the course of conducting such surveys and/or studies. The indemnities herein shall expressly survive the Closing or the termination of this Contract and shall be in addition to any liquidated damage provisions contained in this Contract.
Sample 1
SURVEYS AND STUDIES. A. During the Inspection Period Purchaser shall be permitted to enter the Property and to inspect and evaluate the Property, to conduct studies thereon, and to interview Tenants. If Purchaser determines for an reason that the Property is not suitable for Purchaser’s purposes. Purchaser may terminate this Contract upon written notice to Seller and to Escrow Agent prior to the end of the Inspection Period whereupon the Xxxxxxx Money shall be refunded to Purchaser.
Sample 1
SURVEYS AND STUDIES. As part of the work of the Bioethics Unit, several surveys and studies are regularly conducted. Relevant among them are analyses of the situation of ethical oversight in the re- search funding agencies in the Latin American and Caribbean Region, studies of the biomedical publications, information about legislation with bioethical impact in the countries of the LAC Region, and several projects in association with the Center at the University of Chile (Social representation of genomics, ethical re- view committees and their functioning, among others). The Unit is open to sug- gestions about other information which could be collected and disseminated. Information and publications The Bioethics Unit has maintained publication of the scholarly journal “ Acta Bioethica” (ISSN 0717-5906) published twice a year in monographic format with invited contributions and peer-reviewed articles. The journal is available in electronic PDF format free to download and is sent to all PAHO Represen- tations, universities, and libraries. It also publishes the quarterly newsletter “Bioética Informa” aimed at in- forming about events and developments in the Region (also available in elec- tronic format). Additionally, several books and monographs have been published. It is usual for the International Advisory Board’s meetings to include an academic sec- tion and its members are invited to contribute with papers which are published afterwards in book form. A complete list of those publications, including full- text versions, is available at the website of the Bioethics Unit. Databases used by the Bioethics Unit include RedBIO, a complete listing of persons and institutions, as well as training programs and academic facilities. The Virtual Library on Bioethics, available since several months, was pre- sented in January 2004 for general access and represents one project in con- junction with BIREME. Other joint undertakings include the edition of a se- xxxx of interviews and conferences published as DVD (“Diálogos en Bioética” in English and Spanish, including interviews with prominent bioethicists such as Xxxxx Xxxxxx, Xxxxxx Xxxxxxxx, Xxxxx Xxxxx, Xxxxxxx Xxxxx, Xxx Xxxxxxxx, among others). Two series of “comics” or illustrated stories dealing with selected topics of the history of science and reproductive medicine have been produced in asso- ciation with the University of Chile (“Viajeros Virtuales” and “Entretecho”), funded by the Chilean Commission for Science and Technology and...
Sample 1

Related to SURVEYS AND STUDIES

  • Studies The clinical, pre-clinical and other studies and tests conducted by or on behalf of or sponsored by the Company or its subsidiaries that are described or referred to in the Registration Statement, the Pricing Disclosure Package and the Prospectus were and, if still pending, are being conducted in accordance in all material respects with all statutes, laws, rules and regulations, as applicable (including, without limitation, those administered by the FDA or by any foreign, federal, state or local governmental or regulatory authority performing functions similar to those performed by the FDA). The descriptions of the results of such studies and tests that are described or referred to in the Registration Statement, the Pricing Disclosure Package and the Prospectus are accurate and complete in all material respects and fairly present the published data derived from such studies and tests, and each of the Company and its subsidiaries has no knowledge of other studies or tests the results of which are materially inconsistent with or otherwise call into question the results described or referred to in the Registration Statement, the Pricing Disclosure Package and the Prospectus. Except as described in the Registration Statement, the Pricing Disclosure Package and the Prospectus, neither the Company nor its subsidiaries has received any notices or other correspondence from the FDA or any other foreign, federal, state or local governmental or regulatory authority performing functions similar to those performed by the FDA with respect to any ongoing clinical or pre-clinical studies or tests requiring the termination or suspension of such studies or tests. For the avoidance of doubt, the Company makes no representation or warranty that the results of any studies, tests or preclinical or clinical trials conducted by or on behalf of the Company will be sufficient to obtain governmental approval from the FDA or any foreign, state or local governmental body exercising comparable authority.

  • Environmental Studies Promptly conduct and complete, at Borrower’s expense, all such investigations, studies, samplings and testings as may be requested by Lender or any governmental authority relative to any substance, or any waste or by-product of any substance defined as toxic or a hazardous substance under applicable federal, state, or local law, rule, regulation, order or directive, at or affecting any property or any facility owned, leased or used by Borrower.

  • Clinical Studies The animal and other preclinical studies and clinical trials conducted by the Company or on behalf of the Company were, and, if still pending are, to the Company’s knowledge, being conducted in all material respects in compliance with all Applicable Laws and in accordance with experimental protocols, procedures and controls generally used by qualified experts in the preclinical study and clinical trials of new drugs and biologics as applied to comparable products to those being developed by the Company; the descriptions of the results of such preclinical studies and clinical trials contained in the Registration Statement and the Prospectus are accurate and complete in all material respects, and, except as set forth in the Registration Statement and the Prospectus, the Company has no knowledge of any other clinical trials or preclinical studies, the results of which reasonably call into question the clinical trial or preclinical study results described or referred to in the Registration Statement and the Prospectus when viewed in the context in which such results are described; and the Company has not received any written notices or correspondence from the FDA, the EMA, or any other domestic or foreign governmental agency requiring the termination, suspension or modification of any preclinical studies or clinical trials conducted by or on behalf of the Company that are described in the Registration Statement and the Prospectus or the results of which are referred to in the Registration Statement and the Prospectus.

  • Trials The Ship shall run the following test and trials:

  • Surveys Each Borrower shall submit the Ship owned by it regularly to all periodical or other surveys which may be required for classification purposes and, if so required by the Security Trustee provide the Security Trustee, with copies of all survey reports.

  • Feasibility Each of the Project Budget, the Project Schedule and the Disbursement Schedule is realistic and feasible.

  • Regulatory Filings NYISO and Connecting Transmission Owner shall file this Agreement (and any amendment hereto) with the appropriate Governmental Authority, if required. Any information related to studies for interconnection asserted by Developer to contain Confidential Information shall be treated in accordance with Article 22 of this Agreement and Attachment F to the ISO OATT. If the Developer has executed this Agreement, or any amendment thereto, the Developer shall reasonably cooperate with NYISO and Connecting Transmission Owner with respect to such filing and to provide any information reasonably requested by NYISO and Connecting Transmission Owner needed to comply with Applicable Laws and Regulations.

  • Geotechnical Investigation Perform in accordance with the City Design Manual and other City requirements as designated in writing by the Director.

  • 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.

  • Feasibility Study 4.3.1 The Feasibility Study shall identify any potential adverse system impacts that would result from the interconnection of the Generating Facility.

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