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.
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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. 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.
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. 1.3

Related to CRFs

  • 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. c.

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