Outcomes Progress Reports definition

Outcomes Progress Reports means the Outcomes Progress Reports described in Article D.3.0 (Outcomes Progress Reports).
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Outcomes Progress Reports means the Outcomes Progress Reports described in Article D.4.0 (Outcomes Progress Reports).
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Examples of Outcomes Progress Reports in a sentence

  • The Progress Reports and Final Progress Report are described in Article D.2.0 (Progress Reports and Final Progress Report) and the Outcomes Reports are described in Article D.3.0 (Outcomes Progress Reports).

  • Also, each Outcomes Progress Report will include the information described below in paragraph D.3.1 (a) (Baseline Data (2015) Template) for the first Progress Report and for all other Outcomes Progress Reports.

  • Also, each Outcomes Progress Report will include the information described below in paragraphD.3.1 (a) (Baseline Data (2015) Template) for the first Progress Report and for all other Outcomes Progress Reports.

  • D.3.0 OUTCOMES PROGRESS REPORTS D.3.1 Format and Information for Outcomes Progress Reports.

  • Except for the first Outcomes Progress Report, the Recipient will provide the results on outcomes based on the performance indicators identified below for all Outcomes Progress Reports.

  • The Progress Reports and Final Progress Report are described in Article D.3.0 (Progress Reports and Final Progress Report) and the Outcomes Progress Reports are described in Article D.4.0 (Outcomes Progress Reports).

  • The Recipient will submit Progress Reports, Outcomes Progress Reports and a Final Progress Report to the Province for each Sub-project as required and within the timelines in Schedule “J” (Requests for Payment and Payment Procedures).

  • Along with making some technical amendments and using an updated data set to underpin allocations.

Related to Outcomes Progress Reports

  • Progress Report means the report similar in form and content to that attached hereto as Appendix III.

  • Adverse Event means any untoward medical occurrence in a patient or clinical investigation subject administered a pharmaceutical product and that does not necessarily have a causal relationship with the treatment. An adverse event can therefore be any unfavourable and unintended sign (including an abnormal laboratory finding), symptom, or disease temporally associated with the use of a medicinal product, whether or not related to the medicinal product.