Specimens and Genetic Data Sample Clauses

Specimens and Genetic Data. Sponsor shall have the exclusive right and license to use any and all biological materials and samples, such as blood or tissue, from a Trial Participant collected pursuant to the Protocol (“Specimens”) as well as RNA, DNA, and protein sequence, restriction fragment length polymorphism (RFLP), and similar data collected pursuant to the Protocol (“Genetic Data”). Any use of Genetic Data and/or Specimens, whether such use occurs as part of or outside of the Trial will be in accordance with the Protocol, other written instruction, the informed consent form, and Applicable Law. Sponsor grants Institution and Investigator access to Specimens and Genetic Data only for purposes of the Trial. Investigator shall deliver all Specimens and Genetic Data to Sponsor or its respective designee in a timely manner throughout the performance of the Trial, as provided in the Protocol, in no event later than sixty (60) days following the completion of the Trial by Investigator or the earlier termination of this Agreement. 7.5 Vzorky a genetická data. Zadavatel bude mít výhradní právo a licenci užívat veškeré biologické materiály a vzorky Subjektů hodnocení, například krev nebo tkáně, shromážděné dle Protokolu (xxxx xxx „Vzorky“), jakož i RNA, DNA a proteinové sekvence, polymorfismus délky restrikčních fragmentů (RFLP) a podobné údaje shromážděné dle Protokolu (xxxx xxx „Genetická data“). Veškeré užívání Genetických dat a/nebo Vzorků v rámci nebo mimo rámec Klinického hodnocení musí být vždy v souladu s Protokolem, jinými písemnými pokyny, s formulářem informovaného souhlasu a s Příslušnými právními předpisy. Zadavatel povoluje Zdravotnickému zařízení a Zkoušejícímu přístup ke Vzorkům a Genetickým datům pouze pro účely Klinického hodnocení. Zkoušející bude předávat Zadavateli xxxx xxx ustanovené osobě všechny Vzorky a Genetická data během xxxx xxxx provádění Klinického hodnocení včas, jak je stanoveno v Protokolu, ale v každém případě nejpozději šedesát (60) dní po datu, kdy Zkoušející dokončí Klinické hodnocení, nebo po datu ukončení této Smlouvy, nastane-li dříve.
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Specimens and Genetic Data. Sponsor shall have the exclusive right and license to use any and all biological materials
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Specimens and Genetic Data. Any and all biological materials and samples, such as blood or tissue, from a Trial Participant collected pursuant to the Protocol (“Specimens”) as well as RNA, DNA, and protein sequence, restriction fragment length polymorphism (RFLP), and similar data collected pursuant to the Protocol (“Genetic Data”) shall be solely owned by Sponsor. Any use of Genetic Data and/or Specimens, whether such use occurs as part of or outside of the Trial will be in accordance with the Protocol, other written instruction, the informed consent form, and Applicable Law. Sponsor grants Institution access to Specimens and Genetic Data only for purposes of the Trial. Institution and Investigator shall deliver all Specimens and Genetic Data to Sponsor or its respective designee in a timely manner throughout the performance of the Trial, as provided in the Protocol, in no event later than sixty (60) days following the completion of the Trial by Institution and Investigator or the earlier termination of this Agreement.
Sample 1
Specimens and Genetic Data. Sponsor shall have the exclusive right and license to use any and all biological materials and samples, such as blood or tissue, from a Trial Participant collected pursuant to the Protocol (“Specimens”) as well as RNA, DNA, and protein sequence, restriction fragment length polymorphism (RFLP), and similar data collected pursuant to the Protocol (“Genetic Data”). Any use of Genetic Data and/or Specimens, whether such use occurs as part of or outside of the Trial will be in accordance with the Protocol, other written instruction, the informed consent form, and Applicable Law. Sponsor grants Provider access to Specimens and Genetic Data only for purposes of the Trial. Provider and Investigator shall deliver all Specimens and Genetic Data to Sponsor or its respective designee in a timely manner throughout the performance of the Trial, as provided in the Protocol, in no event later than sixty (60) days following the completion of the Trial by Provider and Investigator or the earlier termination of this Agreement.
Sample 1

Related to Specimens and Genetic Data

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