Initial Phase. The initial phase refers to the period between the initial inquiry and the implementation of the model. A representative of the “initiator” or prospective partner agency requests and receives in-depth information about ParentChild+ implementation. The prospective partner agency, working with the National Center, identifies funding to support the site, develops a budget, signs a replication agreement, and employs a Coordinator. Sites serving more than fifty to sixty families must have a second Coordinator, full-time or part-time depending on the total number of families being served. The Coordinator must be trained by the ParentChild+ National Center or a certified regional training center. The elements described above must all have taken place (i.e. signed replication agreement, required number of trained Coordinators, etc.) before a partner agency can implement the Program.
Initial Phase. Except as otherwise set forth in Section 3.3(b)(iii) below, the initial phase of the Collaboration shall commence on the Effective Date and end four (4) years following the Effective Date (the “Initial Phase”).
Initial Phase. 1 Clinical Trial. Xencor shall be the sponsor of the Ongoing Phase 1 Trial. Xencor shall conduct such trial in accordance with […***…] and the Xencor Development Plan as set forth in Exhibit J as it may be updated in accordance with this Agreement. Xencor shall pay all costs necessary to complete all activities listed in the Xencor Development Plan. The estimated budget for such costs is the amount of […***…] US Dollars ($[…***…]) (the “Budget”). For clarity, if the costs necessary to complete all activities listed in the Xencor Development Plan exceed the Budget, such costs shall be borne by Xencor. Notwithstanding the foregoing, in the event MorphoSys changes any material aspect of the listed activities or includes additional activities in the Xencor Development Plan in accordance with Section 2.2(e)(ii), [...***...]. Xencor shall also bear the costs for additional Licensed Product manufacturing after the Effective Date to supply Xencor’s needs for the Ongoing Phase 1 Trial, to the extent such the Licensed Product from such additional manufacturing is used in the Ongoing Phase 1 Trial. For the costs of the remaining Licensed Product from such additional manufacturing, [...***...] ***Confidential Treatment Requested [...***...], whereby MorphoSys shall use Commercially Reasonable Efforts to use such material. In the event that manufacturing material from the same batch shall be used by Xencor for the Ongoing Phase 1 Trial and by MorphoSys for a clinical trial under its own sponsorship, the Parties shall closely communicate with each other and seek to find the most advantageous way to enable such split of material. In case safety, regulatory or any other issues arise in the course of the Ongoing Phase 1 Trial in relation to which Xencor and/or MorphoSys reasonably conclude that Ongoing Phase 1 Trial should be stopped temporarily or entirely, decision making in such case shall be in accordance with the provisions of Section 2.2(e) (iii). To the full extent permitted by law, Xencor will include MorphoSys in monitoring visits and audits of clinical trials sites (but solely if permitted by the sites), Manufacturer and other Third Parties involved in the Ongoing Phase 1 Trial conduct.
Initial Phase. The period of time from the Go-Live Date until June 30, 2012 or until the Contractor is authorized by the Department to enter the Expansion Phase, whichever is later.
Initial Phase. The Facility shall be constructed in two phases, the Initial Phase and the Final Scope of Work. Great Lakes and the Band agree to proceed with the Design Phase and the Construction Phase of the Initial Phase in accordance with Articles 4 and 5, and to equip the Initial Phase of the Facility in accordance with Article 6. The intent of the parties is to take all steps necessary in accordance with Articles 4 and 5 to permit the Band to commence construction of the Initial Phase immediately upon the taking into trust of the Gaming Site and receipt of NIGC Approval, and to complete construction of the Initial Phase, equip the Initial Phase of the Facility and commence Gaming as soon as reasonably practicable thereafter.
Initial Phase. Clarification phase General Immediately following the conclusion of the Contract, a clarification phase shall be initiated for the purpose of ascertaining whether it is expedient to clarify or supplement the Delivery Description, cf. Appendix 3. Clarification or supplementation of the Delivery Description shall be within the scope of the procurement rules as applicable at any time. To the extent that no agreement can be reached for clarification or supplementation of the Delivery Description and/or other appendices, and the Customer does not wish to exercise its right of withdrawal, cf. clause 4.2, the Delivery Description and the other parts of the Contract shall remain unchanged. The Customer shall notify the Supplier thereof in writing and not later than by the end of the clarification phase. The clarification phase shall be implemented jointly by the Parties in accordance with the time schedule in Appendix 1. The clarification phase shall end when the activities stated in Appendix 1 have been implemented and completed and notification thereof has been submitted in writing by both Parties.
Initial Phase. Initial Phase shall have the meaning contained in the ------------- Program Materials and shall refer to the initial phase of Solicitations under the Program and not any remailings or duplicate Solicitations.
Initial Phase. Notify the Contracting Officer or designated representative when crews are ready to start work on a definable feature of work. Observe the initial segment of the definable feature of work to ensure that the work complies with contract requirements. Document the results of the initial phase in the Daily Contractor Quality Control Report. Repeat the initial phase when acceptable levels of specified quality are not being met. Perform the following for each definable feature of work:
Initial Phase. The period of time from when the Department authorized the Contractor’s RCCO to enter the Initial Phase until June 30, 2012.
Initial Phase. FCS shall have transferred all documentation relating to the FCS Technology to LIFELOC FCS shall have completed the training of two individuals designated by LIFELOC LIFELOC, with the assistance of FCS, shall have completed its purchase of all equipment necessary, as provided by FCS, in connection with the production of Products and shall have the equipment set up In production mode LIFELOC, with the assistance of FCS, shall have made suitable arrangements with all appropriate raw material vendors including substitute vendors from those used by FCS if required. LIFELOC, with the assistance of FCS, shall have established process requirements, processes, and Quality Control procedures in connection with the production of Products.
