Study Standards Sample Clauses

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"). 1.1
Sample 1Sample 2
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Study Standards. Institution 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 clin- ical practice; (v) the International Council on Harmonisation 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 au- thority ("Regulatory Authority") and any other authority that apply to the conduct of the Study or the activities contemplated hereunder ("Applicable Law"). zmocněným k poskytování určitých služeb v souvislosti s Klinickým hodnocením. X. Xxxxxxxx hodnocení je předmětem společného zájmu Smluvních stran a je pro obě Smluvní strany prospěšné, přičemž napomáhá dosažení výzkumných cílů Smluvních stran. D.XXXXXXXXXXXXX, (xxxx označovaný xxx xxxx “Zkoušející”) souhlasí s funkcí hlavního zkoušejícího pro Klinické hodnocení ve Zdravotnickém zařízení, a to na základě separátní smlouvy se společností Idorsia (xxxx označovanou xxx xxxx “Smlouva se zkoušejícím”). E. Zdravotnické zařízení jako pracoviště, kde se provádí klinická hodnoceníí si přeje realizovat činnosti v rámci Klinického hodnocení za podmínek stanovených v této Smlouvě. Smluvní strany se dohodly takto: ČLÁNEK 1 PROVÁDĚNÍ KLINICKÉHO HODNOCENÍ 1.1 Standardy Klinického hodnocení. Zdravotnické zařízení bude provádět Klinické hodnocení v souladu s (i) podmínkami této Smlouvy; (ii) Protokolem; (iii) odůvodněnými písemnými pokyny společnosti Idorsia; (iv) všeobecně přijímanými standardy správné klinické praxe; (v) směrnicí pro správnou klinickou praxi International Council on Harmonization of Technical Requirements of Pharmaceuti- cals for Human Use Guideline for Good Clin- ical Practice (xxxx označovaná xxx xxxx „ICH-GCP“); a (vi) veškerými národními a mezinárodními právními předpisy, vyhláškami, pravidly a směrnicemi jakéhokoli státního úřadu (xxxx označovaného xxx xxxx „Regulační orgán“) a jakéhokoli jiného úřadu, které se vztahují na provádění Klinického hodnocení nebo na činnosti zamýšlené touto Smlouvou (xxxx označované xxx xxxx „Příslušné právní předpisy”). 1.2
Sample 1
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"). 1.1
Sample 1Sample 2
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
Sample 1
Study Standards. The Services will be provided according the options selected and communicated by you (e.g. _Your Test Item Data).
Sample 1
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
Sample 1
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"). 1.1
Sample 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.
Sample 1
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.
Sample 1

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 Xxxxxx pursuant to the Injury and Illness Prevention Program. If applicable, Contractor must receive all health and safety information and training from County.

  • ETHICAL STANDARDS 10.7.1 Within 90 days after the Effective Date, Developer shall adopt written policies establishing ethical standards of conduct for all Developer-Related Entities (other than NTTA), including Developer’s supervisory and management personnel, in dealing with (a) TxDOT and the Independent Engineer and (b) employment relations. Such policy shall be subject to review and comment by TxDOT prior to adoption. Such policy shall include standards of ethical conduct concerning the following:

  • WORKLOAD STANDARDS One (1) Direct Service Hour (DSH) will be equal to sixty (60) minutes of direct services.

  • Development Standards 9.1 Developer shall comply with the requirements contained in the Annexation Agreement and any other duly executed agreement related to the Property, except as specifically amended by this Agreement.

  • Information Technology Accessibility Standards Any information technology related products or services purchased, used or maintained through this Grant must be compatible with the principles and goals contained in the Electronic and Information Technology Accessibility Standards adopted by the Architectural and Transportation Barriers Compliance Board under Section 508 of the federal Rehabilitation Act of 1973 (29 U.S.C. §794d), as amended. The federal Electronic and Information Technology Accessibility Standards can be found at: xxxx://xxx.xxxxxx-xxxxx.xxx/508.htm.

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