Biological Samples means any physical samples obtained from Study Participants in accordance with the Protocol for the purposes of the Study.
Biological Samples means any physical samples obtained from Study Subjects in accordance with the Protocol. Case Report Form means a printed, optical or electronic document or database designed to record all of the information, required by the Protocol on each Study Subject.
Biological Samples means blood, fluid and tissue samples collected from subjects enrolled in the Study, including any tangible materials derived from such samples. The Institution and Investigator will collect, retain, use and transfer Biological Samples only in accordance with the Protocol and the applicable Informed Consent. Institution and Investigator will not collect or reserve additional quantities of Biological Samples for use in research not described in the applicable Protocol. Upon completion or termination of the Study, Institution and Investigator will deliver or dispose of the Biological Samples according to Sponsor's instructions and/or any relevant provisions in the Protocol.
Examples of Biological Samples in a sentence
If the Trial is terminated early as described below, the Agreement will terminate after receipt by Sponsor or CRO of all relevant Protocol-required data, Trial documents and Biological Samples and receipt of all payments due to either Party.
Sponsor or its designees will test Biological Samples as described in the Protocol.
If so specified in the Protocol and if in compliance with Applicable Law and the Trial Subject’s informed consent, Institution and Principal Investigator may collect and provide to Sponsor or its designee Biological Samples (“Biological Samples”).
Institution and Principal Investigator will not use Biological Samples collected under the Protocol in any manner or for any purpose other than that described in the Protocol.
For purposes of this Agreement, the Trial is considered complete after conclusion of all Protocol-required activities for all enrolled Trial Subjects; receipt by Sponsor or CRO of all relevant Protocol-required data, Trial documents and Biological Samples; and receipt of all payments due to either Party.
More Definitions of Biological Samples
Biological Samples means biological samples (e.g., blood, urine, tissue, saliva, etc.) obtained from Trial Subjects.
Biological Samples means blood, fluid and/or tissue samples collected from Subjects as may be set forth in the Protocol, and tangible materials directly or indirectly derived from such samples. “Biologické vzorky” představují vzorky krve, tělesných tekutin a/nebo tkání odebíraných subjektům hodnocení na základě ustanovení protokolu a veškeré hmotné materiály, které jsou z těchto vzorků přímo či nepřímo odvozeny.
Biological Samples means, but is not limited to: bacteria and other microorganisms, bacteria, plant, animal, or any human biological materials, genetic samples, any copies of the original genetic samples, any cell lines containing copies of the original genetic samples, and data derived from these samples.
Biological Samples means the samples (including but not limited to primary tumor tissue (FFPE), metastatic lesion tissue (both frozen and FFPE), whole blood, plasma and serum and derivatives) collected in performance of the Program from Program patients in accordance with the AURORA protocol, to be used to conduct the analyses defined in the AURORA protocol, and later according to the Program Policy for Access to (both clinical and genomic) Data and Biological Samples;
Biological Samples means blood, fluid and/or tissue biopsy samples collected from Study subjects as set forth in the Protocol, and tangible materials directly or indirectly derived from such samples. Institution may collect, retain and/or use Biological Samples solely as ser forth in the Protocol. Institution will provide Sponsor or its designee Biological Samples, as requiered by the Protocol, obtained from Study subjects for testing that is not directly related to patient care or safety monitoring, including pharmacokinetic, pharmacogenomic, or biomarker testing. (h)
Biological Samples. “Biological Samples” means blood, fluid and/or tissue samples collected from Study Subjects as may be set forth in the Protocol, and tangible materials directly or indirectly derived from such samples. Institution and Investigator will collect, retain and/or use Biological Samples solely as set forth in the Protocol. Institution and/or Investigator will provide Sponsor or its designee with quantities of Biological Samples as required by the Protocol. Sponsor may use such Biological Samples as specified in the Protocol, and as permitted in the informed consent form signed by the Study Subjects and by applicable law. 1.10 Survival 1.9 Biologické vzorky „Biologickými vzorky“ se rozumí vzorky krve, tekutin a tkání odebírané Subjektům studie podle Protokolu a hmotné materiály přímo nebo nepřímo získané z takových vzorků. Zdravotnické zařízení a Zkoušející budou Biologické vzorky shromažďovat, uchovávat a používat pouze způsobem stanoveným v Protokolu. Biologické vzorky budou Zdravotnické zařízení a/nebo Zkoušející Zadavateli nebo jím určenému zástupci předávat v množstvích požadovaných Protokolem. Zadavatel může Biologické vzorky používat způsobem stanoveným v Protokolu a k účelům, s nimiž Subjekty studie souhlasily podepsáním formuláře informovaného souhlasu, nebo případně způsobem přípustným podle platných právních předpisů. 1.10
Biological Samples means any physical samples obtained from Study Subjects in accordance with the Clinical Investigation Plan. Case Report Form means a printed, optical or electronic document or database designed to record all of the information, required by the Clinical Investigation Plan, to be reported to the Sponsor on each Study Subject. Clinical Investigator’s brochure means the compilation of the preclinical, clinical and safety information on the Investigational Product relevant to the Clinical Investigation Plan and is as defined in ISO 14155 – 1:2003. Clinical Investigation Plan means the document identified in Schedule 6 which is developed by the Sponsor and clinical investigator(s) that states the rationale, objectives, design and proposed analysis, methodology, monitoring, conduct and record-keeping of the clinical investigation and is as defined in ISO 14155 – 2:2003.