Phase 1 Period definition

Phase 1 Period means the period, on a country-by-country basis, from the Closing Date until the earlier of:
Sample 1Sample 2Sample 3
Phase 1 Period has the meaning given in Exhibit 17, Section 4.2(a). “Phase 2 Period” has the meaning given in Exhibit 17, Section 4.3(a). “Physician Advisory Services” or “PAS” means those Services that are specified in Exhibit 2-B. “Policy and Procedures Manual” means the Policy & Procedures Manual to be prepared in accordance with Section 9.1. “Portal” has the meaning given in Exhibit 2-B, Section 1.
Sample 1
Phase 1 Period means with respect to Lamisil the period, from the Closing Date until the earlier of (a) the MA Transfer Date; and (b) four (4) years from the Closing Date and with respect to Parlodel the period on a product-by-product basis and on a country-by-country basis, from the Closing Date until the earlier of (a) the IDL Transfer Date with respect to China or the MA Transfer Date with respect to Hong Kong and Taiwan; and (b) two (2) years from the Closing Date.
Sample 1

Examples of Phase 1 Period in a sentence

  • Novartis obligation to supply the Product shall be limited to supplying Products in the same form as it was supplied to Novartis and/or its Affiliates or Third Party distributors as of the Closing Date (or during the Phase 1 Period if modified) in the Territory.

  • The Parties acknowledge and agree that neither Party shall undertake marketing and promotional activities in connection with Product Parlodel during the Phase 1 Period.

  • Subject to the conditions set forth in the relevant Third Party Agreement, Novartis shall terminate those Third Party Agreements set forth in Part B of Annex 5 as soon as reasonably practicable after the Closing Date but in any event not before the end of the Phase 1 Period.

  • The Parties acknowledge that, with respect to the Elidel Licensed Product, during the Phase 1 Period (as defined in the Elidel Supply Agreement) with respect to Canada and Mexico, Valeant is not authorized to distribute, sell or invoice the Elidel Licensed Product in such countries and *** or its Affiliates shall continue to distribute such Elidel Licensed Product in such countries during such period, in accordance with the terms of the Elidel Supply Agreement.

  • The Provincial Bidding Before the end of the Phase 1 Period, Novartis shall or cause Novartis’ distributors to continue to participate in the bidding process at the provincial level in connection with the Products in China where Novartis has existing bids as at the date of signature of this Agreement as listed in Annex 6.


More Definitions of Phase 1 Period

Phase 1 Period has the meaning given to it in the Supply Agreement.
Sample 1

Related to Phase 1 Period

  • Completion Period means the period starting from the date of issue of "Order" and required to complete the work in all respect.

  • Production Period is the period that for winter cereal advances commences October 1, 2021 and terminates September 30, 2023; for advances on all other field crops, honey, hogs, goats, sheep and lambs commences April 1, 2022 and terminates September 30, 2023; and for advances on cattle, continuous flow cattle, and bison commences on April 1, 2022 and terminates on March 31, 2024.

  • Peak Period means the time between 6 a.m. and 10 p.m. (April through September) or between 7 a.m. and 11 p.m. (October through March) on all days except Saturdays and Sundays, which daily time period will be subject to change from time to time at the Company's option. This change would occur after no less than ten (10) days notice has been given to all Customers who would be affected, and to the Commission.

  • project completion period means the period of sixty (60) months commencing from and expiring on for the construction and obtaining of Temporary Occupation Permit or Permits for the whole of the Development as provided in clause 3.3;

  • Phase 1 Clinical Trial means a Clinical Trial of a Product on sufficient numbers of normal volunteers and/or patients that is designed to establish that such Product is safe for its intended use and to support its continued testing in Phase 2 Clinical Trials. For purposes of this Agreement, ‘initiation’ of a Phase 1 Clinical Trial for a Product means the first dosing of such Product in a human subject in a Phase 1 Clinical Trial.

  • Ramp Period The Ramp Period shall begin on the Effective Date and continue for a period of 3 months following the Effective Date. Commencing with the Effective Date and at all times during the Ramp Period thereafter, Customer will receive the rates, discounts, charges and credits set forth herein and will not be subject to the AVC. Annual Volume Commitment (“AVC”): $360,000 in Total Service Charges (“AVC”) during each contract year of the Term (following the expiration of the Ramp Period).

  • Initial Period means the period from (and including) the Issue Date to (but excluding) the First Call Date;

  • Commissioning Period means, with respect to each Subproject, the period commencing upon the first delivery of Feed Gas to the Subproject in accordance with Sections 4.8 and 11.1 of the Agreement continuing through achievement of RFSU, commissioning, Start Up, Performance Testing and achievement of Substantial Completion for such Subproject.

  • Development Period means the period from the date of this Agreement until the Appointed Date;

  • Start-up Period means up to 7 Academy Financial Years and covers the period up to and including the first Academy Financial Year in which all age groups are present at the Academy (that is, all the pupil cohorts relevant to the age range of the Academy will have some pupils present).

  • Phase 2 Clinical Trial means a human clinical trial of a product in any country that would satisfy the requirements of 21 C.F.R. 312.21(b) and is intended to explore a variety of doses, dose response, and duration of effect, and to generate initial evidence of clinical safety and activity in a target patient population, or a similar clinical study prescribed by the relevant Regulatory Authorities in a country other than the United States.

  • Evaluation Period bears the meaning ascribed thereto in Section 7.4(d)(i);

  • Annual Period means each twelve (12) month period commencing on the Effective Date and, thereafter, on each anniversary of the Effective Date.

  • Operation Period means the period commencing from COD and ending on the Transfer Date;

  • Research Period means the research period as described in the Commissioned Research Plan. In accordance with the provisions of this Agreement, in the event that the Agreement ended prior to the completion date of the research originally set, the date the Agreement ends shall be read as the research period.

  • Work period means the period specified in a Plan when an employee is at work.

  • First Extension Period means a period of twelve (12) consecutive months following the Initial Maturity Date.

  • Project Year means the 12 month period beginning from the Effective Date and ending 12 months thereafter and each successive 12 month period following thereafter;

  • Planning Period means the 12 moths beginning June 1 and extending through May 31 of the following year, or such other period approved by the Members Committee.

  • Phase III Study means a human clinical trial that is prospectively designed to demonstrate statistically whether a product is safe and effective for use in humans in a manner sufficient to obtain regulatory approval to market such product in patients having the disease or condition being studied as described in 21 C.F.R. § 312.21(c) (FDCA), as amended from time to time, and the foreign equivalent thereof.

  • Operating Period for any Element of the Project shall mean the period from (and including) the COD of such Element of the Project, up to (and including) the Expiry Date and for the Project, shall mean the period from (and including) the COD of the Project, up to (and including) the Expiry Date;

  • PEA Period means the period commencing at 9:30 a.m., Eastern time, on the fifth (5th) Business Day immediately prior to the filing of any post-effective amendment to the Registration Statement (as defined herein) or New Registration Statement (as such term is defined in the Registration Rights Agreement), and ending at 9:30 a.m., Eastern time, on the Business Day immediately following, the effective date of any post-effective amendment to the Registration Statement (as defined herein) or New Registration Statement (as such term is defined in the Registration Rights Agreement).

  • Resolution Extension Period As defined in Section 2.03(b).

  • Phase III Clinical Trial means a large, controlled or uncontrolled Clinical Study that would satisfy the requirements of 21 CFR 312.21(c), intended to gather the additional information about effectiveness and safety that is needed to evaluate the overall benefit-risk relationship of the drug and to provide an adequate basis for physician labeling.

  • Phase I Clinical Trial means a study in humans which provides for the first introduction into humans of a product, conducted in normal volunteers or patients to generate information on product safety, tolerability, pharmacological activity or pharmacokinetics, or otherwise consistent with the requirements of U.S. 21 C.F.R. §312.21(a) or its foreign equivalents.

  • Phase I Study means a study in humans which provides for the first introduction into humans of a product, conducted in healthy volunteers or patients to obtain information on product safety, tolerability, pharmacological activity or pharmacokinetics, as more fully defined in 21 C.F.R. § 312.21(a) (or the non-United States equivalent thereof).