Study Standards Sample Clauses

The Study Standards clause defines the quality and methodology requirements that must be followed when conducting studies or research under an agreement. It typically outlines the specific protocols, industry guidelines, or regulatory standards that the parties must adhere to, such as Good Laboratory Practice (GLP) or Good Clinical Practice (GCP). By establishing clear expectations for how studies are to be performed, this clause ensures consistency, reliability, and compliance, thereby reducing the risk of invalid results or regulatory issues.
Study Standards. Institution and Investigator shall perform the Study in accordance with (i) the terms and conditions of this Agreement; (ii) the Protocol; (iii) Idorsia's reasonable written instructions (iv) generally accepted standards of good clinical practice; (v) the International Council on Harmonization of Technical Requirements of Pharmaceuticals for Human Use Guideline for Good Clinical Practice (“ICH-GCP”); and (vi) all national and international laws, ordinances, rules, and regulations of any governmental authority ("Regulatory Authority") and any other authority that apply to the conduct of the Study or the activities contemplated hereunder ("Applicable Law").
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Study Standards. The Services will be provided according the options selected and communicated by you (e.g. _Your Test Item Data).
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Study Standards. Institution and Investigator shall perform the Study in accordance with (i) the terms and conditions of this Agreement; (ii) the Protocol; (iii) Idorsia's reasonable writ- ten instructions (iv) generally accepted stand- ards of good clinical practice; (v) the Interna- tional Council on Harmonization of Technical Requirements of Pharmaceuticals for Human Use Guideline for Good Clinical Practice (“ICH-GCP”); and (vi) all national and interna- tional laws, ordinances, rules, and regula- tions of any governmental authority ("Regu- latory Authority") and any other authority that apply to the conduct of the Study or the activities contemplated hereunder ("Appli- cable Law").
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Study Standards. Institution and Investigator shall perform the Study in accordance with (i) the terms and conditions of this Agreement; (ii) the Protocol; (iii) Idorsia's reasonable writ- ten instructions (iv) generally accepted 1.1
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Study Standards. Provider shall perform the Study in accordance with (i) the terms and conditions of this Agreement; (ii) the Protocol; (iii) Actelion's reasonable written instructions (iv) generally accepted standards of good clinical practice; (v) the International Council on Harmonization of Technical Requirements of Pharmaceuticals for Human Use Guideline for Good Clinical Practice (“ICH-GCP”); and (vi) all national and international laws in a valid and effective wording, ordinances, rules, and regulations of any governmental authority ("Regulatory Authority") and any other authority that apply to the 1.1 Standardy Klinického hodnocení. Poskytovatel provádí Klinické hodnocení v souladu s (i) podmínkami této Smlouvy; (ii) Protokolem; (iii) odůvodněnými písemnými pokyny společnosti Actelion; (iv) všeobecně přijímanými standardy dobré klinické praxe; (v) směrnicí pro dobrou klinickou praxi International Council on Harmonization of Technical Requirements of Pharmaceuticals for Human Use Guideline for Good Clinical Practice (dále označovaná jen jako „ICH-GCP“); a (vi) veškerými národními a mezinárodními právními předpisy v platném a účinném znění, vyhláškami, pravidly a směrnicemi jakéhokoli státního úřadu (dále conduct of the Study or the activities contemplated hereunder ("Applicable Law"). označovaný jen jako „Regulační orgán“) a jakéhokoli jiného úřadu, které se vztahují na provádění Klinického hodnocení nebo na činnosti zamýšlené touto Smlouvou (dále označované jen jako „Příslušné právní předpisy“).
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Study Standards. Institution and Investigator shall perform the Study in accordance with (i) the terms and conditions of this iv) generally accepted standards of good clinical practice; (v) the International Council on Harmonization of Technical Requirements of Pharmaceuticals for Human Use Guideline for Good Clinical Practice (“ICH-GCP”); and (vi) all national and international laws, ordinances, rules ( e.g. relevant legislation, SÚKL's requirements), and regulations of any governmental authority ("Regulatory Authority") and any other authority that apply to the conduct of the Study or the activities contemplated hereunder ("Applicable Law").
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Study Standards. Institution and Investigator shall perform the Study in accordance with (i) the terms and conditions of this Agreement; (ii) the Protocol; (iii) Idorsia's reasonable written instructions (iv) generally accepted standards of good clinical practice; (v) the International Council on Harmonization of Technical Requirements of Pharmaceuticals for Human Use Guideline for Good Clinical Practice (“ICH-GCP”); and (vi) with all relevant laws of the Czech Republic, in particular Act No. 378/2007 Coll., on Pharmaceuticals and on Amendments to Certain Related Acts (the Pharmaceuticals Act), Act No. 372/2011 Coll., on Health Services as amended, including the implementing regulations to these laws (in particular Decree No. 226/2008 Coll., establishing good clinical practice.rules, and regulations of State Institute for drug control ("Regulatory Authority") and any other authority that apply to the conduct of the Study or the activities contemplated hereunder 1.1
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Study Standards. In performing the Supplemental Review, PNM will use appropriate electric utility practices to determine whether the GF can be interconnected to the EPS safely and reliably. Each Party will perform its obligations as set forth in this Agreement in a manner that reflects best practices in the electric industry and that are consistent with regional practices, applicable laws and regulations, and the organizational nature of each Party. All of the terms and provisions, to the extent practicable, shall be consistent with the provisions of Rule 568.
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Study Standards. The study procedure will use Good Utility Practice and the engineering and operating principles, standards, guidelines and criteria of the Transmission Provider, the Regional Reliability Council of which the Transmission Provider is a member, any entity of which the Transmission Provider is a member and is approved by the Commission to promulgate or apply regional or national planning and reliability standards (such as a regional transmission group, RTG), NERC or any similar organization that may exist in the future of which the Transmission Provider is then a member. In all cases, system addition(s) to the electric supply facilities shall maintain or improve the Transmission Provider’s transmission system operation, reliability and transfer capability.
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Related to Study Standards

  • Safety Standards Performance of the Contract for all commodities or contractual services must comply with requirements of the Occupational Safety and Health Act and other applicable State of Florida and federal requirements.

  • Quality Standards Each Party agrees that the nature and quality of its products and services supplied in connection with the other Party's Marks will conform to quality standards set by the other Party. Each Party agrees to supply the other Party, upon request, with a reasonable number of samples of any Materials publicly disseminated by such Party which utilize the other Party's Marks. Each Party will comply with all applicable laws, regulations, and customs and obtain any required government approvals pertaining to use of the other Party's marks.

  • OMB Standards Unless specified otherwise within this agreement, the Subrecipient shall procure all materials, property, or services in accordance with the requirements of 24 CFR 84.40−48.

  • Technical Standards The Generation System shall be installed and operated by the Interconnection Customer consistent with the requirements of this Agreement; the Technical Requirements; the applicable requirements located in the National Electrical Code (NEC); the applicable standards published by the American National Standards Institute (ANSI) and the Institute of Electrical and Electronic Engineers (IEEE); and local building and other applicable ordinances in effect at the time of the installation of the Generation System.

  • Health and Safety Standards Contractor shall abide by all health and safety standards set forth by the State of California and/or the County of ▇▇▇▇▇▇ pursuant to the Injury and Illness Prevention Program. If applicable, Contractor must receive all health and safety information and training from County.