Archaeological Investigations Sample Clauses

Archaeological Investigations. The conduct of archaeological activities, including without limitation survey, excavation and artifact retrieval, following submission of an archaeological field investigation plan and its approval in writing by Xxxxxxx and the State Archaeologist of the Massachusetts Historical Commission (or appropriate successor official).
Sample 1
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Archaeological Investigations. A. The archaeological investigations must be performed by or under the direct supervision of an archaeologist(s) who qualifies under the Secretary of the Interior's Professional Qualification Standards set out at 48 FR 44716, September 29, 1983, for Archaeology. Archaeological fieldwork and associated reporting will follow the Louisiana Division of Archaeology’s Phase II Site Testing Standards, xxxx://xxx.xxx.xxxxx.xx.xx/archaeology/review/phase_II_site_testing_xxxxxxxxxx.xx px .
Sample 1
Archaeological Investigations. The Scoping Study prepared for the Town concluded: The proposed location of the sidewalk on the east side of Bridge Street has previously been disturbed from utility installation and preparation for storm drain installation. The Old Village Cemetery was established on rise above the street level, so no burials would be anticipated within the project area. No further archeological investigation is recommended for this portion of the sidewalk improvement project. However, if the project team determines that further investigations (such as the use of ground- penetrating radar or similar non-invasive methods) are prudent to determine if gravesites will potentially be impacted by the construction, these services can be added to this scope of work under a supplemental agreement.
Sample 1
Archaeological Investigations. The Consultant shall be responsible for the archaeological investigations and will conclude any specific contracts with authorised entities, in accordance with legal requirements on the archaeological standards and procedures, set out in Chapter 2-3, of the Order of Ministry of Culture and Religious Affairs no. 2392/2004. Thus, based on the planned archaeological works the Consultant shall carry out the following aspects: Completion of a Desk Study (Theoretical Evaluation) (to be completed at route option stage): • Carry out research into any historical data (documents, photos, maps sketches, etc.) and review any relevant references to existing literature; • Development of an archaeological topography study correlated with the proposed route options including the preferred route; • Assess the likely position and extent of the archaeological sites, prepare estimates of the likely costs and duration of the archaeological discharge activities envisaged for each route option and consider this aspect as part of the multi criteria assessment, which shall be carried out. Completion of the Field Investigations (Required for the Preferred Route) • Performance of aerial photogrammetric investigations; • Performance of geophysical investigations; • Performance of a detailed field exploration (known as periegheza) and of archaeological surveys for the entire route of the future motorway; • The performance of a predictive pattern (regarding the distribution of the archaeological patrimony sites) in certain areas. This is to be achieved through the correlation of archive and field investigation data, with preparation of the main documentation validating areas of low archaeological risk. Drafting of an Assessment Report (Diagnostic Study) which must comprise: • Distribution in plan with clear delineation of the sites that shall be impacted by the future highway project, in STEREO 70 coordinates including GIS registration; • Classification of archaeological sites through significance of sites and the prioritisation of sites based on the need for further in depth research; • Identification and planning of specific measures for the attenuation of impacts on archaeological patrimony, summarised in a management plan; • Proposing a preventive archaeological research methodology adapted to the actual situation on site; • Assessment of the necessary costs for envisaged preventive archaeological research, the structure of the research team and the development of a works schedule,...
Sample 1
Archaeological Investigations. A. Within 30 days after the date of this Agreement, the City shall engage Commonwealth Heritage Group or with a Cultural Resource Firm ("CRF") that meets the Secretary of Interior's standards for an PAGE 2 OF 10 MPIIBS/MPC PROPERTY AGRMT. 2019 AGREEMENT archeological professional, to undertake an archaeological investigation of the portions of the City Property currently designated as Category B and Category C areas.
Sample 1

Related to Archaeological Investigations

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

  • Environmental Investigation (a) Acquiror may, in its discretion, within thirty (30) Business Days of the date of this Agreement, require the Company to order, at Acquiror’s expense, a Phase I environmental site assessment to be delivered only to Acquiror for each parcel of real property in which the Company or an Acquired Subsidiary holds an interest or formerly held an interest (each a “Phase I Report”), conducted by an independent professional consultant reasonably acceptable to Acquiror to determine if any real property in which the Company or any Acquired Subsidiary holds any interest or formerly held an interest contains or gives evidence of any adverse environmental condition or any violations of Environmental Laws on any such property. If a Phase I Report discloses any violations or adverse environmental conditions, or reports a reasonable suspicion thereof, then Acquiror may promptly obtain, at the expense of the Company and Acquiror, shared equally, a Phase II environmental report with respect to any affected property which report shall contain an estimate of the cost of any remediation or other follow-up work that may be necessary to address those violations or conditions in accordance with applicable laws and regulations (each a “Phase II Report,” and collectively referred to with the associated Phase I Report, an “Environmental Report”). Acquiror shall have no duty to act upon any information produced by an Environmental Report for the benefit of the Company, any Acquired Subsidiary or any other Person, but shall provide such information to the Company upon the Company’s request.

  • Cooperation with Investigations You agree to cooperate with us in the investigation of unusual transactions, poor quality transmissions, and resolution of customer claims, including by providing, upon request and without further cost, any originals or copies of items deposited through the Service in your possession and your records relating to such items and transmissions.

  • Background Investigation The BOARD is prohibited from knowingly employing a person who has been convicted of committing or attempting to commit certain criminal offenses. If the required criminal background investigation is not completed at the time this Contract is signed, and the subsequent investigation report reveals that there has been a prohibited conviction, this Contract shall immediately become null and void.

  • COMPLAINTS AND INVESTIGATIONS 1. This article applies to complaints or allegations made externally and not from normal supervisory activities.

  • Complaints Investigation ‌ An employee who complains of harassment under the provisions of the Human Rights Code of British Columbia may refer the complaint to either one or other of the following processes:

  • Formal Investigation Once the matter has been brought to the attention of the Store executive, an internal investigation of the complaint will be conducted at which time the complainant will be requested to present, in writing, the particulars of the harassment. Such internal investigation will be initiated no later than ten (10) business days of the matter being brought to the attention of the Store executive, and shall be concluded no later than thirty (30) business days of the initiation of the investigation. Any extension of the aforementioned time frames must have the agreement of the complainant and the union if the complainant has chosen to involve it. Based on the outcome of the investigation, which will be provided in writing upon the completion of the investigation, to both the complainant and the union, should the complainant consent to this disclosure, it will be determined if there has been a breach of Company policy on harassment, and the appropriate action will be taken in the event that harassment is determined to have occurred. STEP THREE - SUBSEQUENT INCIDENTS Subsequent incidents should immediately be reported and followed by a written description to the most senior store executive involved in Step Two for further investigation and disciplinary action, if confirmed, with a copy to the union Chairperson with the consent of the complainant. After all steps of the Harassment Protection Policy have been exhausted, if the incident has not been resolved to the satisfaction of the employee, the employee may file a grievance at Step 2 of the grievance procedure.

  • Investigations; Litigation There is no investigation or review pending (or, to the knowledge of Parent, threatened) by any Governmental Entity with respect to Parent or any of its Subsidiaries which would have, individually or in the aggregate, a Parent Material Adverse Effect, and there are no actions, suits, inquiries, investigations or proceedings pending (or, to Parent’s knowledge, threatened) against or affecting Parent or its Subsidiaries, or any of their respective properties at law or in equity before, and there are no orders, judgments or decrees of, or before, any Governmental Entity, in each case which would have, individually or in the aggregate, a Parent Material Adverse Effect.

  • TECHNOLOGY/KNOWLEDGE TRANSFER ACTIVITIES The goal of this task is to develop a plan to make the knowledge gained, experimental results, and lessons learned available to the public and key decision makers. The Recipient shall: • Prepare an Initial Fact Sheet at start of the project that describes the project. Use the format provided by the CAM. • Prepare a Final Project Fact Sheet at the project’s conclusion that discusses results. Use the format provided by the CAM. • Prepare a Technology/Knowledge Transfer Plan that includes: o An explanation of how the knowledge gained from the project will be made available to the public, including the targeted market sector and potential outreach to end users, utilities, regulatory agencies, and others.

  • 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.

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