Electronic Data Capture Clause Samples

The Electronic Data Capture clause establishes the use of digital systems for collecting, storing, and managing data related to a project or transaction. Typically, this clause outlines the specific platforms or software to be used, the responsibilities of each party in entering and maintaining data, and any requirements for data security or access. By formalizing the process of electronic data management, the clause ensures accuracy, efficiency, and traceability, reducing the risk of data loss or errors associated with manual record-keeping.
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Electronic Data Capture. The electronic data capture (EDC) system is a secure, validated, US CFR Part 11 compliant EDC program provided by the Sponsor. It is an internet-based EDC system for reporting clinical data to the Sponsor (eCRFs). All subjects who consent to participate will be registered in the EDC system. Access to the EDC system will be protected by login identification and password. The Sponsor will train delegated Site personnel on procedures for data entry into the web-based system. Following, delegated staff will be provided ID codes and passwords unique to each team member’s delegated study role and blinding requirements. They will be trained on Philips guidelines for maintenance of electronic ID codes and passwords. A staff member’s ID code/password will never be shared or used by another staff member, in any circumstance.
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Electronic Data Capture. ‌ Some types of studies may require methods of data collection in addition to, or instead of, CRFs. For example, questions about a study participant’s sexual behavior or drug use may best be collected using a computerized questionnaire methodology such as an “[Audio]- Computer Assisted Self-Interview” ([A]CASI). The protocol team and SDMC will assess whether additional methods of data capture are required and if so, whether the SDMC, a contractor, or some other Network resource will be responsible for designing the required system. If the SDMC develops the system, development will follow steps similar to the design of CRFs.
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Electronic Data Capture. Institution and Principal Investigator acknowledge that Sponsor may retain one or more companies to provide services involving electronic document and data collection, retention and processing associated with the performance of a Clinical Trial. Institution covenants that it shall (a) own or have access to space, computer hardware and internet connectivity necessary to operate an Electronic Data Capture (“EDC”) terminal that will permit the input of relevant Clinical Trial data and documents and transmission of the same between Institution and Sponsor’s designee, and (b) train and maintain sufficient and appropriate staff and personnel in the operation of the EDC terminal. In such cases, Institution shall ensure that the applicable Principal Investigator will, during the Clinical Trial and throughout the term of this Agreement, be familiar with the operation of the EDC terminal and supervise the staff and personnel who are operating the same. poskytovat součinnost Zadavateli v téže souvislosti.
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Electronic Data Capture. Institution and Principal Investigator acknowledge that Company may retain one or more companies to provide services involving electronic document and data collection, retention and
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Electronic Data Capture. Provider and Principal Investigator acknowledge that Sponsor may retain one or more companies to provide services involving electronic document and data collection, retention and Zadavatelem v souladu s Pšíslušnými právními pšedpisy. Hlavní zkoušející je povinen evidovat takový dokument v souladu s vnitšními pravidly Poskytovatele, pšičemž poskytne jeho kopii Zadavateli na jeho žádost. Žádný Subjekt hodnocení nebude zašazen do Klinického hodnocení, nebyl-li pšedtím opatšen jeho písemný infomovaný souhlas.
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Electronic Data Capture. Institution and Principal Investigator acknowledge that Company may retain one or more companies to provide services involving electronic document and data collection, retention and processing associated with the performance of a Clinical Trial. Institution covenants that it shall (a) own or have access to space, computer hardware and internet connectivity necessary to operate an Electronic Data Capture (“EDC”) terminal that will permit the input of relevant Clinical Trial data and documents and transmission of the same between Institution and Company’s designee, and (b) train and maintain sufficient and appropriate staff and personnel in the operation of the EDC terminal. In such cases, Institution shall ensure that the applicable Principal Investigator will, during the Clinical Trial and throughout the term of this Agreement, be familiar with the operation of the EDC terminal and supervise the staff and personnel who are operating the same. s tímto Klinickým hodnocením, a to včetně vyjednání smluv o klinickém hodnocení s jednotlivými ▇▇▇▇▇ výkonu klinického hodnocení, resp. centry, jménem a ve prospěch Společnosti. Instituce souhlasí, že zajistí, že Hlavní zkoušející a personál zapojený do provádění Klinického hodnocení poskytnou plnou součinnost CRO, a to z pozice smluvní výzkumné organizace jednající jménem Společnosti ve vztahu ke Klinickému hodnocení (a případně zástupci či zmocněnci CRO, dle konkrétních podmínek), stejně jako jsou Instituce a Hlavní zkoušející povinni spolupracovat a poskytovat součinnost Společnosti v téže souvislosti. 1.5
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Related to Electronic Data Capture

  • Electronic Data 7.1.1 The parties recognize that Contract Documents, including drawings, specifications and three-dimensional modeling (such as Building Information Models) and other Work Product may be transmitted among Owner, Design-Builder and others in electronic media as an alternative to paper hard copies (collectively “Electronic Data”).

  • Electronic Data Interchange If both Parties elect to facilitate business activities hereunder by electronically sending and receiving data in agreed formats (also referred to as Electronic Data Interchange or “EDI”) in substitution for conventional paper-based documents, the terms and conditions of this Agreement shall apply to such EDI activities.

  • Electronic Data Interchange (EDI This standard establishes the data contents of the Invoice Transaction Set (810) for use within the context of an EDI environment. This transaction set can be used for invoicing via the AN for catalog and non-catalog goods and services.

  • Electronic Devices No electronic devices that may hinder job performance or safety (especially cell phones), may be carried on employees’ person, or be used by employees during working hours.

  • ELECTRONIC WORKFLOW SYSTEM OGS reserves the right to incorporate an electronic workflow system that may include elements of the Authorized User RFQ process. OGS reserves the right to post Authorized User Contract usage of Centralized Contracts. For Lot 4 only, when provided for in the RFQ and resultant Authorized User Agreement, the Authorized Users may reimburse travel expenses. All rules and regulations associated with this travel can be found at ▇▇▇▇://▇▇▇.▇▇▇▇▇.▇▇.▇▇/agencies/travel/travel.htm. In no case will any travel reimbursement be charged that exceeds these rates. All travel will be paid only as specified within the Authorized User Agreement and must be billed with the associated services on the same Invoice with receipts attached. The Contractor shall receive prior approval from the Authorized User for any travel that occurs during the term of an Authorized User Agreement. Parking fees and/or parking tickets shall not be paid by an Authorized User. Unless otherwise specified in writing by the Authorized User, a vehicle will not be provided by Authorized User to the Contractor for travel. Therefore, the Contractor will be responsible for ensuring that the Contractor has access to an appropriate vehicle (e.g., personal vehicle or rental vehicle) or common carrier with which to carry out any necessary travel. For the Contractor to obtain reimbursement for the use of a rental vehicle, such use must be justified as the most cost- effective mode of transportation under the circumstances (including consideration of the most effective use of time). The Contractor is responsible for keeping adequate records to substantiate any claims for travel reimbursement. All services provided under the resultant Authorized User Agreement must be performed within CONUS. There are no BONDS for this Contract. However, an Authorized User may require in an RFQ a performance, payment or Bid bond, or negotiable irrevocable letter of credit or other form of security for the faithful performance for the resultant Authorized User Agreement. Pursuant to New York State Executive Law Article 15-A and Parts 140-145 of Title 5 of the New York Codes, Rules and Regulations (“NYCRR”), the New York State Office of General Services (“OGS”) is required to promote opportunities for the maximum feasible participation of New York State-certified Minority- and Women-owned Business Enterprises (“MWBEs”) and the employment of minority group members and women in the performance of OGS contracts.