GCP Sample Clauses

The GCP (Good Clinical Practice) clause establishes the requirement for all parties involved in clinical research to adhere to internationally recognized ethical and scientific quality standards. This clause typically mandates that clinical trials be conducted in accordance with GCP guidelines, which cover aspects such as protocol compliance, informed consent, data integrity, and participant safety. By enforcing these standards, the clause ensures the reliability of clinical trial results and the protection of human subjects, addressing regulatory compliance and ethical concerns in clinical research.
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GCP. Verbal agreements shall only be valid if the Client con- firms them in writing. Purchase orders shall be con- firmed by the Contractor in writing without undue delay. If the Contractor does not confirm the Purchase order in writing within 14 calendar days of receipt, the Client shall be entitled to revoke it.
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GCP. The Client shall make available to the Contractor information con- cerning compliance with the obligations under Sec. 9 para. 5.1 to 5.3 GCP within two weeks of the simple request of such information.
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GCP. The term “
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GCP. The Client is entitled to rights of set-off (Aufrechnung) and retention (Zurückbehaltungsrecht) as well as the defense of non-performance of the contract (Einrede des nicht erfüllten Vertrages) to the extent provided by law. In particular, the Client shall be entitled to withhold payments due as long as the Client is still entitled to claims against the Contractor arising from incomplete or defective services.
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GCP. Zkoušející a zdravotnické zařízení se zavazují uschovat veškerou dokumentaci o provedení klinického hodnocení i dokumentaci vztahující se k subjektům hodnocení až do doby, kdy zadavatel nebo společnost ICON oznámí zkoušejícímu či zdravotnickému zařízení, že další uschovávání dokumentace není potřeba, nejméně však po dobu 5 let od data ukončení klinického hodnocení. Identifikační kódy subjektů hodnocení budou zdravotnické zařízení/zkoušející uchovávat nejméně po dobu 15 let. Pro případ, že prvotní údaje budou dostupné pouze v elektronické podobě, zavazuje se zkoušející pro účely jejich ověření pořídit výtisky všech dat, která se týkají subjektů hodnocení a jsou významná pro klinické hodnocení. Tyto výtisky budou opatřeny to make a print out of all data related to the trial subjects relevant to the clinical Study. These print-outs will be dated and signed by the Investigator and duly retained as source documents. datem a podpisem zkoušejícího a řádně uschovány.
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GCP. The term "GCP" shall mean the applicable current good clinical practices promulgated from time to time by the FDA in accordance with the Act, and which may be amended from time to time (or the equivalent in any foreign country).
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GCP. The parties agree that Client’s sole payment obligations for the Service are contained in the GCP Marketplace Agreement. Client may not use or access the Service if Client does not comply with all of its payment obligations specified in the GCP Marketplace Agreement.
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Related to GCP

  • Good Industry Practice all applicable Standards; and

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  • Development Standards For any structure built on the Property following the Effective Date, it shall comply with the requirements contained in Exhibit B, “Building Materials,” attached hereto and incorporated herein. The Parties agree and acknowledge that the provisions of this Paragraph shall apply to any structure constructed subsequent to the execution of this Agreement. Nothing in this Agreement shall be deemed to modify or otherwise amend any zoning regulation duly adopted by the Town, previously or in the future.

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