CRFs Sample Clauses

CRFs. (1) The CRFs shall be paid by Vendor to DIR for each direct sales transaction un- der the CTSA. The CRF per direct sales transaction Service is specified in the CTSA at Exhibit C. Payment of the CRFs shall be due on the thirtieth (30th) calendar day after the close of the previous month period. (2) Vendor shall reference the CTSA contract number on any remittance instru- ments.
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CRFs. All case report forms and other data (including without limitation, written, printed, graphic, video, image, and audio material, and information contained in any computer database or computer readable form) created or developed during the course of the Study by Participating Site (excluding source records) (the “Data”) shall be the property of EAN, which may utilize the Data in any way it deems appropriate, subject to and in accordance with applicable Laws and Regulations and the terms of this Agreement.
CRFs. Site shall complete case report forms (“CRFs”) following visits by Study subjects in accordance with the Protocol. If electronic CRFs are used, Investigator shall attest to the validity of Investigator’s electronic signatures on such CRFs by signing an acknowledgement.
CRFs. If additional corrections are needed, the responsible monitor or Data Manager will raise a query. The appropriate investigational staff will answer queries sent to the Investigator. In case screen failure data is entered in the (e)CRF, these data should be clearly indicated in the raw datasets and removed from the analysis datasets.
CRFs. USOR shall cause Study Personnel to input Study data on electronic CRFs using the electronic system provided by BIND promptly following data collection. Each Site shall prevent unauthorized access of the data by maintaining physical security of the computers and maintaining the confidentiality of their passwords. Each Site shall respond within seven (7) business days to BIND’s queries. If a Site is unable to resolve a query within this timeframe, it will instead respond to BIND with an explanation in writing and continue to resolve such query within a reasonable time period.
CRFs. Completed, adequate and accurate CRFs shall be provided to Cato Research Ltd., SPONSOR designee and contract research organizations required in the PROTOCOL and otherwise as reasonably requested by SPONSOR or its designee. In the event that subject follow-up is not possible for any reason, this fact and the circumstances thereof shall be documented in the CRF.

Related to CRFs

  • Project Records Borrower shall: Make and keep books, records, and accounts, in such reasonable detail, so as to fully, accurately, and fairly reflect the activities of Borrower. Record the Project’s assets, liabilities, revenues, expenses, receipts and disbursements in separate accounts from any other assets, liabilities, revenues, expenses, receipts and disbursements of Borrower so as to permit the production of a Statement of Financial Position, a Statement of Profit and Loss (Statement of Activities), and a Statement of Cash Flows for Borrower in which the activities of Borrower are separately identifiable from the activities of the Operator, unless Borrower is also Operator. Devise and maintain a system of internal accounting controls sufficient to provide reasonable assurances that: Transactions are executed, and access to assets is permitted, only in accordance with Xxxxxxxx’s authorization; Transactions are accurately and timely recorded to permit the preparation of quarterly and annual financial reports in conformity with applicable Program Obligations; Transactions are timely recorded in sufficient detail so as to permit an efficient audit of the Borrower’s books and records in accordance with Generally Accepted Auditing Standards (GAAS), Generally Accepted Government Auditing Standards (GAGAS), and other applicable Program Obligations; and Transactions are timely recorded in sufficient detail so as to maintain accountability of the Borrower’s assets. The recorded accountability for assets shall be compared with the existing assets at reasonable intervals, but not less than annually, and appropriate action shall be taken with respect to any differences. Make the books, records and accounts of Borrower available for inspection by HUD or its authorized representatives, after reasonable prior notice, during normal business hours, at the Project or other mutually agreeable location or, at HUD’s request, shall provide legible copies of such documents to HUD or its authorized representatives within a reasonable time after HUD or its authorized representative makes a request for such documents. Include as a requirement in any operating or management contract that the books, records, and accounts of any agent of Borrower, as they pertain to the operations of the Project, shall be kept in accordance with the requirements of this Section 19 and be available for examination by HUD or its authorized representatives after reasonable prior notice during customary business hours at the Project or other mutually agreeable location or, at HUD’s request, the Management Agent shall provide legible copies of such documents to HUD or its authorized representatives within a reasonable time after HUD or its authorized representative makes the request.

  • Medical Records Medical records relating to Trial Subjects that are not submitted to Sponsor may include some of the same information as is included in Trial Data; however, Sponsor makes no claim of ownership to those documents or the information they contain.

  • Patient Records Upon termination of this Agreement, the New PC shall retain all patient dental records maintained by the New PC or the MSO in the name of the New PC. During the term of this Agreement, and thereafter, the New PC or its designee shall have reasonable access during normal business hours to the New PC's and the MSO's records, including, but not limited to, records of collections, expenses and disbursements as kept by the MSO in performing the MSO's obligations under this Agreement, and the New PC may copy any or all such records.

  • Study Population Infants who underwent creation of an enterostomy receiving postoperative care and awaiting enterostomy closure: to be assessed for eligibility: n = 201 to be assigned to the study: n = 106 to be analysed: n = 106 Duration of intervention per patient of the intervention group: 6 weeks between enterostomy creation and enterostomy closure Follow-up per patient: 3 months, 6 months and 12 months post enterostomy closure, following enterostomy closure (12-month follow-up only applicable for patients that are recruited early enough to complete this follow-up within the 48 month of overall study duration).

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