Common use of Operator Obligations Clause in Contracts

Operator Obligations. (a) The Operator shall obtain copies of the IPC Standards described in Section 1.1(a) of this Schedule from time to time during the Term from the Minister‟s website at ▇▇▇▇://▇▇▇.▇▇▇▇▇▇.▇▇▇▇▇▇▇.▇▇/newsroom/pub-infection-prevention.html (b) The Operator shall obtain information about the approval and licensing of reusable medical devices under Section 1.1(b) of this Schedule from Health Canada or by consulting Health Canada‟s website at: ▇▇▇.▇▇-▇▇.▇▇.▇▇/▇▇▇-▇▇▇/▇▇▇▇▇▇▇▇▇▇▇/▇▇-▇▇_▇.▇▇▇▇ (c) In accordance with Sections 3.2 and 9.4 of the Sterilization Standards, the Operator shall obtain approval from AHS‟ Infection Prevention and Control executive appointed pursuant to the Sterilization Standards: (i) prior to reprocessing medical devices outside of a centralized reprocessing area; and (ii) prior to purchasing any new sterilizer.

Operator Obligations. (a) The Operator shall obtain copies of the IPC Standards described in Section 1.1(a) of this Schedule from time to time during the Term from the Minister‟s website at ▇▇▇▇://▇▇▇.▇▇▇▇▇▇.▇▇▇▇▇▇▇.▇▇/newsroom/pub-infection-prevention.html (b) The Operator shall obtain information about the approval and licensing of reusable medical devices under Section 1.1(b) of this Schedule from Health Canada or by consulting Health Canada‟s website at: ▇▇▇.▇▇-▇▇.▇▇.▇▇/▇▇▇-▇▇▇/▇▇▇▇▇▇▇▇▇▇▇/▇▇-▇▇_▇.▇▇▇▇- im_e.html (c) In accordance with Sections 3.2 and 9.4 of the Sterilization Standards, the Operator shall obtain approval from AHS‟ Infection Prevention and Control executive appointed pursuant to the Sterilization Standards: (i) prior to reprocessing medical devices outside of a centralized reprocessing area; and (ii) prior to purchasing any new sterilizer.

Operator Obligations. (a) The Operator shall obtain copies of the IPC Standards described in Section 1.1(a) of this Schedule from time to time during the Term from the Minister‟s Minister’s website at ▇▇▇▇://▇▇▇.▇▇▇▇▇▇.▇▇▇▇▇▇▇.▇▇/newsroom/pub-infection-prevention.html (b) The Operator shall obtain information about the approval and licensing of reusable medical devices under Section 1.1(b) of this Schedule from Health Canada or by consulting Health Canada‟s Canada’s website at: ▇▇▇.▇▇-▇▇.▇▇.▇▇/▇▇▇-▇▇▇/▇▇▇▇▇▇▇▇▇▇▇/▇▇-▇▇_▇.▇▇▇▇- im_e.html (c) In accordance with Sections 3.2 and 9.4 of the Sterilization Standards, the Operator shall obtain approval from AHS‟ AHS’ Infection Prevention and Control executive appointed pursuant to the Sterilization Standards: (i) prior to reprocessing medical devices outside of a centralized reprocessing area; and (ii) prior to purchasing any new sterilizer.