Specific Responsibilities of the JRC. In addition to its general responsibilities, the JRC shall, subject to the terms of this Agreement, in particular:
(a) review and discuss the progress of the Research Plan; and discuss, prepare and approve for submission to the JSC any proposed amendments to the Research Plan;
(b) discuss the use of Delivery Technology with respect to Opt-In Products and Collaboration Products under this Agreement;
(c) discuss when the formation of a JDC would be appropriate given the stage of research for the Opt-In Products; and
(d) perform such other functions as may be appropriate to further the purposes of this Agreement, as directed by the JSC or as set forth under this Agreement.
Specific Responsibilities of the JRC. As part of its overall responsibilities described in section 3.1, the JRC will:
(i) review the progress of the Research activities, and if necessary, propose and approve changes to the Research Plan;
(ii) review and approve any changes to the allocation of responsibility for Research costs;
(iii) review and approve the strategy for the filing, prosecution, and maintenance of the ACI Patent Rights, Xxxxxxx Patent Rights or Joint Patent Rights; and
(iv) perform such other functions as appropriate to further the purposes of this Agreement as determined by the Parties.
Specific Responsibilities of the JRC. Without limiting the generality of Section 2.1.3(d), the JSC (or, if such authority is granted to the JRC by the JSC, the JRC) shall:
(i) manage the operationalization of the Preclinical Research Plan, and propose changes and updates to the Preclinical Research Plan (including the then-current Preclinical Research Budget); and
(ii) monitor, review and record the progress of the activities under the Preclinical Research Plan.
Specific Responsibilities of the JRC. The responsibilities of the JRC will be to:
(a) coordinate the Collaboration Activities;
(b) develop, discuss, and submit to the JSC to further review, discuss, and determine whether to approve each Drug Discovery Plan, and any updates thereto, pursuant to Section 2.2.2 (Additional Drug Discovery Plans) and Section 2.2.3 (Amendments to the Drug Discovery Plans);
(c) develop, discuss, and submit to the JSC to further review, discuss, and determine whether to approve any updates to the Exploratory Research Plan or Exploratory Research Budget, pursuant to Section 2.3.2 (Amendments to the Exploratory Research Plan); and
(d) perform such other functions as determined by the JSC.
Specific Responsibilities of the JRC. The JRC shall have the following responsibilities:
Specific Responsibilities of the JRC. In addition to its overall responsibility for the Research Program, the JRC shall, in particular, during the Research Term (including any Extended Research Term):
(i) oversee the activities of the Working Group;
(ii) resolve any disputes or disagreements relating to the Research Program that are submitted to it by the Working Group or a Party;
(iii) modify the Research Plan as necessary, but in no event shall such modification increase the *** or be contrary to the intent and purpose of this Agreement;
(iv) determine the status of the Research Program to meet the Objective, including determination of success, failure and whether the Research Program cannot, or should not, be further progressed; in determining whether the Research Program can, or should, be further progressed, the JRC may consider factors such as commercial factors and risks related to the Research Target and safety concerns among others; and
(v) review of Program Inventions and the filing of Program Patents. Other than the obligations under (i), (ii) and (iv) above, the JRC may delegate its obligations under this Agreement to the Working Group or any other subcommittee.
Specific Responsibilities of the JRC. The responsibilities of the JRC will be to:
(a) oversee the execution of the Research Plan;
(b) coordinate the Research Activities and facilitate communications between the Parties with respect to the Research Activities;
(c) review, discuss, and determine whether to approve updates to the Research Plan;
(d) review and discuss the results of performance of the Research Activities under the Research Plan, including all reports provided by the Parties, and the anticipated timeline for initiating and completing all activities set forth in the Research Plan;
(e) perform such other functions as appropriate to further the purposes of this Agreement, as expressly set forth in this Agreement, or allocated to it by the Parties’ written agreement.
Specific Responsibilities of the JRC. The JRC shall serve as a forum for overseeing and governing the Research Programs in accordance with the procedures set forth in this Section 4.10 and any other procedures as agreed upon by the JRC members. Except as otherwise provided herein, the role of the JRC shall be to:
(i) exchange information and facilitate discussions and cooperation between the Parties with respect to activities conducted under the Research Programs;
(ii) monitor, review and record the progress of the Research Programs;
(iii) review and approve any Research Plans or updates or amendments to the Research Plans, including criteria for Research Program Deliverables;
(iv) facilitate the activities of the Gatekeeper; and
(v) carry out any other functions delegated to it by the Parties.
Specific Responsibilities of the JRC. The responsibilities of the JRC will be to: (a) coordinate the Collaboration Activities;
Specific Responsibilities of the JRC. In addition to its general responsibilities, the JRC shall in particular:
(i) discuss the requirements for Regulatory Approval in the Territory and oversee and coordinate regulatory matters with respect to Products in the Territory;
(ii) facilitate the flow of Information between the Parties with respect to obtaining Regulatory Approval for Products;
(iii) discuss and manage (along with the JMC) CMC related activities and responses to FDA queries;
(iv) coordinate the preparation for submission of the NDA and XXXx for Products;
(v) manage the transfer of the NDA and INDs for the Initial Dimebon Product to Partner after the Initial Approval Date; and
(vi) perform such other functions as may be appropriate to further the purposes of this Agreement, as directed by the JSC.
