Sea Trials definition

Sea Trials shall have the meaning set forth in Article 7 hereof.
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Sea Trials. Trials as outlined in Article 4 and in the Specifications.
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Sea Trials means trials conducted outside the harbour limits;
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Examples of Sea Trials in a sentence

  • Subject to Clause 27(d) (Sea Trials – Method of Acceptance or Rejection) the Vessel shall be delivered to the Buyer in full and complete compliance with the Contract on the Delivery Date.

  • The Builder shall give the Owner written notice approximately four weeks before anticipated Sea Trials.

  • The Builder shall also give written confirmation of the actual commencement date of the Sea Trials seven (7) days prior thereto.

  • In such case the Sea Trials shall be reasonably postponed to enable the participation of the Owner.

  • The Sea Trials shall be performed in the presence of the Owner’s Sea Trials Committee (the name of whose members shall be provided to the Builder in writing) and the Classification Society’s representatives.

  • In such case, the result of the Sea Trials executed by the Builder and confirmed by the Classification Society's representatives shall signify successful completion of the Sea Trials.

  • In the event of the failure of the Owner's Sea Trial Representative to be present at the Sea Trials after due notice has been given to the Owner as provided above, the Builder may conduct the Sea Trials despite the absence of the Owner's Sea Trial Committee.

  • The Sea Trials shall be performed in the presence of the Owner's Sea Trials Committee (the name of whose members shall be provided to the Builder in writing) and the Classification Society's representatives.

  • The Vessel shall be properly equipped during Sea Trials with sufficient life saving appliances and equipment for the number of persons onboard.

  • In such case, the result of the Sea Trials executed by the Builder and confirmed by the Classification Society’s representatives shall signify successful completion of the Sea Trials.


More Definitions of Sea Trials

Sea Trials means those trials as described in Section 13.1(c) and in the Specifications.
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Sea Trials means trials conducted outside the harbour limits; “spouse” will, when required, be interpreted to include “common-law partner” except, for the purposes of the Foreign Service Directives, the definition of “spouse” will remain as specified in Directive of the Foreign Service Directives;
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Sea Trials means trials conducted outside the harbour limits; "straight-timerate" means the hourly rate of pay;
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Sea Trials means trials conducted outside the harbour limits (« essais en mer »);
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Related to Sea Trials

  • Clinical Studies means Xxxxx 0, Xxxxx 0, Xxxxx 0, Xxxxx 3, and such other tests and studies in human subjects that are required by Applicable Law, or otherwise recommended by the Regulatory Authorities, to obtain or maintain Regulatory Approvals for a Licensed Product for one (1) or more indications, including tests or studies that are intended to expand the Product Labeling for such Licensed Product with respect to such indication.

  • Clinical Trial means a Phase I Clinical Trial, Phase II Clinical Trial or Phase III Clinical Trial, or any post-approval human clinical trial, as applicable.

  • Study means the investigation to be conducted in accordance with the Protocol.

  • Phase 3 Clinical Trial means a pivotal clinical trial in humans performed to gain evidence with statistical significance of the efficacy of a product in a target population, and to obtain expanded evidence of safety for such product that is needed to evaluate the overall benefit-risk relationship of such product, to form the basis for approval of an NDA and to provide an adequate basis for physician labeling, as described in 21 C.F.R. § 312.21(c) or the corresponding regulation in jurisdictions other than the United States.

  • Clinical Study means a Phase I Study, Phase II Study, Phase III Study, as applicable.

  • Phase 3 Trial means a human clinical trial of a Product on a sufficient number of subjects that is designed to establish that a pharmaceutical product is safe and efficacious for its intended use, and to determine warnings, precautions and adverse reactions that are associated with such pharmaceutical product in the dosage range to be prescribed, which trial is intended to support Approval of a Product, as described in 21 C.F.R. 312.21(c) for the United States, or a similar clinical study prescribed by the Regulatory Authorities in a foreign country.

  • Phase 2 Clinical Trial means a human clinical trial, for which the primary endpoints include a determination of dose ranges or an indication of efficacy in patients being studied as described in 21 C.F.R. §312.21(b), or an equivalent clinical trial in a country in the Territory other than the United States.

  • Phase 1 Clinical Trial means a human clinical trial that is intended to initially evaluate the safety and/or pharmacological effect of Licensed Product or that would otherwise satisfy the requirements of 21 C.F.R. 312.21(a) or an equivalent clinical trial in a country in the Territory other than the United States.

  • Pivotal Clinical Trial means a human clinical trial of a Licensed Product that (a) would satisfy the requirements of 21 C.F.R. 312.21(c) or corresponding foreign regulations; or (b) that is intended to provide sufficient efficacy data to support the Filing of a BLA for such Licensed Product in such country. A Pivotal Clinical Trial includes a Phase 2 Clinical Trial or Phase 3 Clinical Trial that satisfies the foregoing definition.

  • Phase I Trial means a clinical trial of a Licensed Product in human patients conducted primarily for the purpose of determining the safety, tolerability and preliminary activity of the Licensed Product, including, without limitation, for determining the maximum tolerated dose, or optimal dose. For purposes of this Agreement, a Phase I trial shall specifically exclude a study in healthy volunteers.

  • 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 2 Trial means a human clinical trial conducted on study subjects with the disease or condition being studied for the principal purpose of achieving a preliminary determination of efficacy or appropriate dosage ranges, as further described in 21 C.F.R. §312.21(b) (including any such clinical study in any country other than the United States).

  • Phase II Clinical Trial means a controlled human clinical study that would satisfy the requirements of 21 CFR 312.21(b), conducted to study the effectiveness and establish the dose range of a Product for a particular Indication in patients with the disease or condition under study, including a Phase IIA Clinical Study or Phase IIB Clinical Study.

  • 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.