Research Site(s) definition

Research Site(s) means a site that is cooperating with a Research Collaborator and, through that cooperation, is participating in the Study.
View Source

Examples of Research Site(s) in a sentence

  • Collaborator will assist the international Clinical Research Sites with the submission of other necessary regulatory documents to allow for such participation.

  • The international Clinical Research Sites will work directly with the Collaborator to obtain the necessary regulatory documents.

  • For clarification purposes, references herein to contractual obligations of Participating Sites shall include the requirement that each Research Collaborator impose such obligations upon its Research Sites.

  • The Company will provide specific storage and/or shipping instructions for the Test Article to the CTSN DCC and the Clinical Research Sites, who will be responsible for adhering to them, as mutually agreed by the Parties.

  • NSABP may provide, or permit Participating Sites to provide, Confidential Information to (a) Research Collaborators and their Research Sites, (b) EC/IRBs and Study Personnel, and (c) applicable accreditation organizations (including their respective agents and representatives).

  • The Company warrants that any packaging for hazardous material, provided by the Company, meets Department of Transportation regulatory requirements for use at all Clinical Research Sites.

  • The Clinical Research Sites will be instructed to follow all applicable laws, regulations and policies regarding the disposition or destruction of the Test Article.

  • If the Test Article must be replaced, the Company will replace it at no cost to NIAID, the Distributor or the Clinical Research Sites.

  • In addition, subject to Section 12.4 of this Agreement, the Company will not enter into any separate agreements, including, but not limited to Material Transfer Agreements, with the Clinical Research Sites or the Investigators at the Clinical Research Sites that interfere with the conduct of this Clinical Trial.

  • The Company will supply sufficient quantities of appropriately formulated Test Article to the Clinical Research Sites without cost or expense, on a schedule mutually agreed upon by the Parties per Attachment 1, which is hereby NHLBI Extramural Clinical Trial Agreement (Cooperative Agreement) CTSN DCC Protocol # CTSNLVAD02 Mesoblast – DCVS, NHLBI July 2014 incorporated in its entirety into this Agreement, to ensure timely performance and completion of the Protocol.