Clinical Trials Database definition

Clinical Trials Database has the meaning ascribed to such term in Section 3.1.3.2.
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Examples of Clinical Trials Database in a sentence

  • AD shall use its commercially reasonable efforts to list clinical trials on behalf of third Persons in the Listing of Clinical Trials Database to the extent such clinical trials are not already included in the Listing of Clinical Trials Database, where AD becomes aware of any such listing.

  • AD hereby acknowledges that the Trials Volunteer Questionnaire Database, the E-mail Notification Service and the Listing of Clinical Trials Database are the exclusive property of CW and AD's rights to such databases and the information incorporated therein are limited to the terms and conditions of this Agreement.

  • SFJ with regard to European Clinical Trial Countries and the SFJ Territory and PB with regard to the US will promptly update the Clinical Trials Database upon receiving data for the Clinical Trials from any Site and any other applicable Permitted Third Party, and each Party will ensure that the Sites and such other Permitted Third Parties promptly following collection thereof, provide data in connection with the Clinical Trials to such Party.

  • AD shall use commercially reasonable efforts to, subject to the terms herein, contract with certain Person concerning recruitment of clinical trial candidates and CW shall comply with the requests of any such Person that lists information in the Listing of Clinical Trials Databases for modifying the information listed in the Listing of Clinical Trials Database by such Person.

  • Pfizer hereby agrees that it shall review Section D of the European Clinical Trials Database (EudraCT) Application Form [***] Certain information in this document has been excluded pursuant to Regulation S-K, Item 601(b)(10).

Related to Clinical Trials Database

  • Clinical Trials means a controlled study in humans of the safety or efficacy of a Product, and includes, without limitation, such clinical trials as are designed to support expanded labeling or to satisfy the requirements of an Agency in connection with any Product Approval and any other human study used in research and Development of a Product.

  • 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.

  • Clinical Studies means human clinical trials for a Licensed Product and any other tests and studies for a Licensed Product in human subjects.

  • Phase III Clinical Trials means a Clinical Trial for the Product on sufficient numbers of patients to generate safety and efficacy data to support Regulatory Approval in the proposed therapeutic indication, conducted in accordance with current good clinical practices and in accordance with a protocol that has been reviewed by the FDA and reflects any comments or concerns raised by the same.

  • 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.