Source Documentation definition

Source Documentation means an original document that contains the details of a marihuana business transaction.

Source Documentation means collection logs and other information developed, maintained and transferred pursuant to Section 18660.20(h) of this Chapter that demonstrates the eligibility, originating generator and/or intermediate handlers of collected CEWs as applicable.

Source Documentation. ’ shall mean a document which shall include the name and legal address of the firewood producer or firewood dealer, the source of the firewood, and the approximate volume of firewood if greater than one cord or 128 cubic feet. Source documentation may consist of a bill of lading, purchase receipt or invoice accompanying all such firewood sold or a label attached to each package or bundle of firewood.

Examples of Source Documentation in a sentence

• Cite or attach Source Documentation: Is the community participating in the National Insurance Program (or has less than one year passed since FEMAnotification of Special Flood Hazards)?Yes.

• The Division of AIDS (DAIDS) policies on Requirements for Source Documentation in DAIDS Funded and/or Sponsored Clinical Trials and Requirements for Essential Documents at Clinical Research Sites Conducting DAIDS Funded and/or Sponsored Clinical Trials are useful for interpreting and operationalizing the regulations and guidelines in accordance with DAIDS expectations.

• Does the project involve acquisition, construction, or rehabilitation of structures located in a FEMA‐identified Special Flood Hazard Area (SFHA)?No. Cite or attach Source Documentation: [Proceed with project.]Yes.

• Does the project involve the sale or acquisition of property located within a Civil Airport Runway Clear Zone or a Military Airfield Clear Zone?No. Cite or attach Source Documentation: [Project complies with 24 CFR 51.303(a)(3).]Yes.

• All DAIDS policies referenced in this section are available at: https://www.niaid.nih.gov/research/daids-clinical-research-policies-standard-procedures Study sites must comply with DAIDS policies on Requirements for Essential Documents at Clinical Research Sites Conducting DAIDS Funded and/or Sponsored Clinical Trials and Requirements for Source Documentation in DAIDS Funded and/or Sponsored Clinical Trials.

More Definitions of Source Documentation

Source Documentation means the medium upon which evidence of a transaction is initially recorded. Examples of source documents include, but are not limited to, purchase requisitions, purchase orders, purchase of service authorizations, staffing schedules, employee hourly time reports, invoices and attendance documents for regional center consumers and all other persons provided services. Source documents are used to prepare records and reports.

Source Documentation means hard copy documentation which proves a person’s eligibility.

Source Documentation means source code comments and other works describing the internal structure and operation of particular source code, including, but not limited to all related specifications, schematics, logic manuals, flow charts, and principals of operation, related build procedures, test harnesses, test procedures, bug data base and design documentation, as available. Documentation may be in tangible form or machine-readable text or graphic files subject to display or printout.

Source Documentation means documentation necessary for Egenera to have the Emulex Product manufactured. Source Documentation includes the Emulex Product approved vendor list; schematics; costed xxxx of materials, quality and reliability data; DVT, DFM, and DFT; packaging data; engineering change orders; and process flows.

Source Documentation means the documentation, including flow charts, annotations, schematics and other explanatory material, relating to the Source Code.

Source Documentation means the documentation accompanying each of the Source Codes.

Source Documentation. The Parties acknowledge and agree that as of the Amendment Effective Date, Novartis has provided QED with legacy safety data from the Novartis global safety database for the Product to enable QED to establish the Global Safety Database (the “GSDB”) for the Product, and such transfer of data from Novartis to QED did not contain any source documentation on safety cases. The Parties acknowledge and agree that Novartis has provided legacy safety data source documentation upon the request of QED where required for patient safety or regulatory reasons for the Products. In accordance with the terms of [***], on November 12, 2021, QED subsequently transferred the GSDB to [***]. Novartis hereby agrees that following the Amendment Effective Date, Novartis shall provide in a timely manner either to QED or to both QED and [***], as QED’s designee, source documentation and audit trail data for an individual case as reasonably requested by QED, [***], or the relevant Regulatory Authorities for patient safety or regulatory reasons for the Product,. QED or [***] will reach out to the Novartis point of contact [***]. Any source documents requiring transfer shall be transferred in compliance with data privacy laws and regulations, and copies of anonymized source documents shall be provided only after redaction of patient and reporter identifiers. Where required, this will be conducted at the expense of QED. No correspondence, communications, or meetings (including in connection with responses to relevant regulatory agencies) will be conducted by Novartis and [***] without the participation of QED as a necessary party. Any source documentation shall be maintained by the Parties, and Novartis’ obligations set forth in this Section 5.4, shall survive expiration or termination of this Agreement, in each case, for at least [***] after the last country has withdrawn the Product from the market, or after a development project ends.”