Study Plan Sample Clauses

Study Plan. The Signatory Companies will submit a Study Plan prepared pursuant to this ECA to EPA at least forty-five (45) days prior to the initiation of testing in accordance with 40 C.F.R. § 790.62 and no more than one hundred twenty (120) days after the effective date of the ECA. The content of the Study Plan submitted to EPA will comply with 40 C.F.R. § 790.62(b). Modifications to the study plan will be governed by the procedures of 40 C.F.R. § 790.62(c). The Study Plan will become part of the official record (docket number EPA-HQ-▇▇▇▇-▇▇▇▇-▇▇▇▇). EPA shall approve the Study Plan at the same time QAPP approval is required if it meets the requirements of this ECA and 40 C.F.R. § 790.62(b). The Study Plan shall become the “Final Study Plan” when approved by EPA. The Signatory Companies shall submit a QAPP to EPA within one hundred eighty (180) days of the Effective Date of this ECA and at least forty-five (45) days prior to the initiation of testing. The QAPP must be prepared in accordance with EPA guidance.1 The QAPP shall include complete information on the Test Standards to be used. If multiple commercial testing laboratories are used for different environmental media and environmental matrices tested, the QAPP will address inter-laboratory variability of D4 analyses. EPA shall approve the QAPP within 60 days of receipt of the QAPP if it meets the requirements of this ECA and is consistent with EPA guidance noted above.

Study Plan. During the Term, FibroGen and Fortis will conduct the collaboration activities in accordance with a study plan (“Study Plan”). The Study Plan will include and be limited to (a) research, CMC, non-clinical development, clinical development, and regulatory activities to be conducted by each Party in support of Development of the Products to achieve the objectives in Article 2 (such activities in the Study Plan, “Development Activities”) and (b) other research and development activities to evaluate the Products and derivatives of the Products (including Modified Products) that FibroGen elects to perform (such activities in the Study Plan, the “Evaluation Activities”), and (c) the allocation of responsibility, as between the Parties, and any timelines with respect to the activities in clause (a) and (b). The current Study Plan is attached hereto as Exhibit A. The Parties will only be permitted to perform Development activities with respect to the Products and Modified Products to the extent included in or otherwise described within the Study Plan. Either Party may submit proposed amendments to the Study Plan from time to time for review and approval by the JSC, and will be effective [*] and incorporated into this Agreement.

Study Plan. On May 15, 2001, PacifiCorp submitted to the agencies for technical review a draft study plan analyzing the feasibility, costs, and benefits of this restoration measure. The agencies shall complete a technical review and provide comments on the draft study plan to PacifiCorp by June 15, 2001. PacifiCorp shall finalize the study plan by June 29, 2001 and distribute it to the agencies and to FERC for inclusion in its NEPA process for the New License.

Study Plan. The detailed study plan for the Pilot Collaboration is attached hereto as Appendix 1 (“Study Plan”). The Parties will conduct the Pilot Collaboration in accordance with the Study Plan with oversight by the JRC. Subject to Section 3.1.4 (g), the Study Plan may only be modified by written agreement of the Parties; provided that the Study Plan shall at all times set forth (a) the three Parts of the Pilot Collaboration and a list of defined success criteria (“Success Criteria”) for each Part, (b) the work to be performed by Synlogic and/or Roche, (c) the Material(s) to be provided by Roche to Synlogic and by Synlogic to Roche, respectively, (d) the expected Deliverables, including data packages, to be provided by each Party during the Pilot Collaboration.

Study Plan. The Parties acknowledge and agree that the Study Plan attached hereto as of the Effective Date sets forth the goals and objectives of the Study. The Parties further acknowledge and agree that the Study Plan may be amended by a unanimous decision of the SMC from time to time during the Term as necessary in the judgment of the SMC.

Study Plan. Total credit requirement for the Masters degree under this remains the same as that of Regular AIT Masters degree in Agribusiness Management (SERD) (26 Cr Course + 22 Cr Thesis = 48 Cr). AIT Faculty will be responsible for AIT courses irrespective of the place of offering; i.

Study Plan. Promptly after (a) in the case of a Triple Combination Product, payment of the first to be paid of the [...***...], but in any event no later than [...***...] days after such payment, and (b) in the case of the Potentiator Product, AbbVie’s election under Section 3.16.3(i) and payment of the [...***...], but in any event no later than [...***...] days after such payment, Galapagos shall transfer to AbbVie, in electronic format, the complete contents of the safety database maintained by Galapagos pursuant to Section 8.2.1 for the applicable Molecules and Products, and thereafter AbbVie shall maintain in accordance with Applicable Law (at AbbVie’s sole cost and expense, but subject to the last sentence of this subsection) the global safety database for each of the applicable Molecules and Products. AbbVie’s and its Affiliates’ costs incurred in connection with receiving, recording, reviewing, communicating, reporting, and responding to adverse events in the Co-Promotion Territory shall be included in Allowable Expenses calculated on an FTE Cost and direct out-of-pocket basis.

Study Plan. The Study Plan must indicate the activities in which the student shall be registered for each semester and/or year of the Agreement, including the thesis defence. As the student must meet the requirements of each PhD program, the Study Plan must indicate if (and which) activities in one program are recognized as equivalent in the other program (recognition of prior learning); it is understood at the outset that the thesis defence shall be acknowledged by both institutions. The Study Plan must state that the student will complete the 3 stages of the PhD exam (research problem, written exam, oral exam). One of the last two stages can be done remotely (written exam or oral exam).

Study Plan. Students can choose where to enter the dual degree program. If they enter at EPOKA, they will spend the first year in Tirana and the second year in Cassino. If they enter the program at UNICAS, they will spend the first year in Cassino, and the second year in EPOKA. The study plans are jointly defined and attached to this agreement (Annex 1).