GSK CANADA'S RESPONSIBILITIES Sample Clauses

GSK CANADA'S RESPONSIBILITIES. GSK Canada shall at its own expense prepare, file and prosecute in its name all relevant regulatory filings for Products in the Territory. GSK Canada shall also be the holder of the NDSs, DINs, DELs and other applicable regulatory filings and approval documents for the Product in the Territory, and will at its own expense, be responsible for all administrative matters necessary to compile and submit the NDSs and other applicable regulatory filings for the Product in the Territory. GSK Canada shall also be responsible for maintaining the NDSs, DINs, DELs and other applicable regulatory filings and approval documents and will bear the registration renewal fees for the NDSs, DINs, DELs and other applicable regulatory filings and approval documents of the Product in the Territory. GSK Canada will keep Corixa informed of its regulatory activities regarding the Product in the Territory on an ongoing and timely basis not less than once each calendar quarter, unless no regulatory activities were conducted in the quarter. In addition, GSK Canada shall provide Corixa with drafts of all regulatory filings, including NDSs and other applicable regulatory filings, at least 60 days before they are filed except for: (i) the NDS prepared pursuant to the LOI, which GSK Canada shall provide to Corixa in installments as soon as practically possible and with a reasonable time to review, and (ii) any regulatory filing that is in response to an inquiry from Health Canada and for which the response deadline is less than 90 days after such inquiry, in which case GSK Canada shall provide the draft regulatory filing to Corixa a reasonable time in advance of filing. Corixa shall have the right to comment thereon, provided that it does so within the response deadline, and GSK Canada shall revise the draft before filing to implement all reasonable Corixa comments.
Sample 1
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GSK CANADA'S RESPONSIBILITIES. GSK Canada shall at its own expense prepare, file and prosecute in its name all relevant regulatory filings for Products in the Territory. GSK Canada shall also be the holder of the NDSs, DINs, DELs and other applicable regulatory filings and approval documents for the Product in the Territory, and will at its own ---------------------------------- * Confidential Treatment requested. Redacted
Sample 1

Related to GSK CANADA'S RESPONSIBILITIES

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  • Other Responsibilities The Responsibility factors also take account of any responsibility the jobholder may have through the provision of advice and guidance on policies and procedures, research or the adaptation or development of existing or new policies and procedures. An assessment tool has been developed to help ensure that advisory, policy and similar ‘hands off’ responsibilities, such as research or democratic services, are correctly measured and allocated to the appropriate Responsibility factor. It is recommended that jobs are first evaluated on their ‘hands on’ responsibilities under each Responsibility factor and that an assessment is then made of the level of advisory/policy responsibilities and the factor to which it should be allocated.

  • Customer Responsibilities Customer shall:

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  • Company Responsibilities The Company will undertake responsibilities as set forth below:

  • General Responsibilities Issuer hereby engages Distributor to act as exclusive distributor of the shares of each class of the Funds. The Funds subject to this Agreement as of the date hereof are identified on SCHEDULE A, which may be amended from time to time in accordance with Section 11 below. Sales of a Fund's shares shall be made only to investors residing in those states in which such Fund is registered. After effectiveness of each Fund’s registration statement, Distributor will hold itself available to receive, as agent for the Fund, and will receive by mail, telex, telephone, or such other method as may be agreed upon between Distributor and Issuer, orders for the purchase of Fund shares, and will accept or reject such orders on behalf of the Fund in accordance with the provisions of the applicable Fund’s prospectus. Distributor will be available to transmit orders, as promptly as possible after it accepts such orders, to the Fund’s transfer agent for processing at the shares’ net asset value next determined in accordance with the prospectuses.

  • Joint Responsibilities 2.1.1 University and Affiliate each will identify, and notify each other of, a person responsible for serving as its liaison during the course of this affiliation. The appointment of liaisons shall be subject to mutual approval of the parties.

  • Development Responsibilities Unless the Parties agree in writing upon an alternate allocation of responsibility, the Parties shall have the following rights and obligations with respect to operational responsibilities under each Development Plan:

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