Monitoring and Data Sample Clauses

Monitoring and Data. Verification Institution/Investigator warrant that Pharm-Olam and Sponsor have access to Study documentation, including records on any pharmacy dispensing the 5. Monitoring a overenie dát Zdravotnícke zariadenie / Skúšajúci zaručujú, že Pharm-Olam a Zadávateľ budú mať prístup ku Študijnej dokumentácii, vrátane záznamov výdaja Investigational Product, comparator and ancillary drugs (if applicable) during normal business hours to monitor the conduct of the Study, including the receipt, handling, storage and dispensing of the Investigational Product comparator and ancillary drugs (if applicable), as well as to audit records, CRFs and source documents. The representatives of Pharm-Olam and Sponsor upon prior notice and during normal business hours shall have access to CRFs (or eCRF); Trial Subjects clinical notes and other relevant Trial Subject information for the purposes of monitoring in compliance with ICH/GCP. Investigator and Institution warrant that they will fully cooperate with Pharm-Olam and Sponsor during monitoring and data verification. The Institution agrees to allow direct access to hospital records and all Trial Subject data relevant to the Study, however stored, for the purpose of Source Document Verification (SDV) by representatives of Pharm-Olam or Sponsor. The Investigator also agrees to provide any missing information in the CRFs (or eCRF), correct any data errors, and complete hospital records in order to ensure that CRF records shall be absolutely consistent with data found in the source data. Skúšaného lieku, referenčnej vzorky, doplnkového liečiva (ak sa budú vydávať) zo strany Lekárne, počas obvyklých pracovných hodín, na monitorovanie výkonu Štúdie, vrátane prevzatia, nakladania, uskladnenia a výdaja Skúšaného lieku, referenčnej vzorky, doplnkového liečiva (ak sa budú vydávať), rovnako ako k auditu záznamov, CRF a zdrojovým dokumentom. Zástupcovia spoločnosti Pharm-Olam a Zadávateľa po predchádzajúcom písomnom oznámení a počas obvyklých pracovných hodín budú mať prístup k CRF (alebo eCRF), klinickým záznamom Subjektu klinického skúšania a iným relevantným informáciám o Subjekte klinického skúšania za účelom vykonanie monitoringu Štúdie v súlade s ICH/GCP. Zdravotnícke zariadenie a Skúšajúci zaručujú, že budú plne spolupracovať so spoločnosťou Pharm-Olam a Zadávateľom v rámci monitoringu a overovania údajov. Zdravotnícke zariadenie súhlasí s umožnením priameho prístupu zástupcom spoločnosti Pharm-Olam alebo Zadávateľa k nemocničným zá...
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Monitoring and Data a. ADS Contact Spreadsheet b. ADS Training Information Spreadsheet
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Monitoring and Data a. ADS Contact Spreadsheet
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Related to Monitoring and Data

  • Monitoring and Review 5.1 The Council and the BID Company shall set up the Standard Services Review Panel within 28 days from the date of this Agreement the purpose of which shall be to:

  • Program Monitoring and Evaluation (c) The Recipient shall prepare, or cause to be prepared, and furnish to the Association not later than six months after the Closing Date, a report of such scope and in such detail as the Association shall reasonably request, on the execution of the Program, the performance by the Recipient and the Association of their respective obligations under the Legal Agreements and the accomplishment of the purposes of the Financing.”

  • Monitoring and Evaluation a. The AGENCY shall expeditiously provide to the COUNTY upon request, all data needed for the purpose of monitoring, evaluating and/or auditing the program(s). This data shall include, but not be limited to, clients served, services provided, outcomes achieved, information on materials and services delivered, and any other data required, in the sole discretion of the COUNTY, that may be required to adequately monitor and evaluate the services provided under this Contract. Monitoring shall be performed in accordance with COUNTY’S established Noncompliance Standards, a copy of which is attached hereto and incorporated by reference as Attachment “C”.

  • Monitoring and Compliance Every year during the term of this Agreement on the anniversary date of the effective date of the Agreement, the Restaurant shall provide to the United States a narrative report of the actions taken during the reporting period to remove any barriers to access and otherwise enhance accessibility for individuals with disabilities at the Restaurant and any plans for action concerning ADA compliance in the coming year. The report shall include as an exhibit copies of any complaint, whether formal or informal, received during the reporting period alleging that the Restaurant was not being operated in compliance with the ADA or otherwise discriminated against any person on account of disability. The Owner and Operator of the Restaurant shall cooperate in good faith with any and all reasonable requests by the United States for access to the Restaurant and for information and documents concerning the Restaurant's compliance with this Agreement and the ADA. The United States shall have the right to verify compliance with this Agreement and the ADA, both as set forth in this Agreement and through any means available to the general public, including visits to the public areas of the Restaurant and communications with Restaurant staff. The United States shall have the right to inspect the facility at any time, and counsel for the United States need not identify themselves in the course of visits to the public areas.

  • Monitoring and Reporting 3.1 The Contractor shall provide workforce monitoring data as detailed in paragraph 3.2 of this Schedule 8. A template for data collected in paragraphs 3.2, 3.3 and 3.4 will be provided by the Authority. Completed templates for the Contractor and each Sub-contractor will be submitted by the Contractor with the Diversity and Equality Delivery Plan within six (6) Months of the Commencement Date and annually thereafter. Contractors are required to provide workforce monitoring data for the workforce involved in delivery of the Contract. Data relating to the wider Contractor workforce and wider Sub-contractors workforce would however be well received by the Authority. Contractors and any Sub-contractors are required to submit percentage figures only in response to paragraphs 3.2(a), 3.2(b) and 3.2(c).

  • Safeguards Monitoring and Reporting 8. The Borrower shall do the following or cause the Project Executing Agency to do the following:

  • Reporting and Monitoring Please provide a brief description of the mechanisms proposed for this project for reporting to the UNDP and partners, including a reporting schedule.

  • Project Monitoring Reporting and Evaluation The Recipient shall furnish to the Association each Project Report not later than forty-five (45) days after the end of each calendar semester, covering the calendar semester.

  • Monitoring and Audit Seller shall provide information on available audit logs and reports relating to cyber and physical and security. Company may audit Seller's records to ensure Seller's compliance with the terms of this Section 1(b)(iii)G (Critical Infrastructure Protection) of this Attachment B (Facility Owned by Seller), provided that Company has provided reasonable notice to Seller and any such records of Seller's will be treated by Company as confidential.

  • Evaluation, Testing, and Monitoring 1. The System Agency may review, test, evaluate and monitor Grantee’s Products and services, as well as associated documentation and technical support for compliance with the Accessibility Standards. Review, testing, evaluation and monitoring may be conducted before and after the award of a contract. Testing and monitoring may include user acceptance testing. Neither the review, testing (including acceptance testing), evaluation or monitoring of any Product or service, nor the absence of review, testing, evaluation or monitoring, will result in a waiver of the State’s right to contest the Grantee’s assertion of compliance with the Accessibility Standards.

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