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").
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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).
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 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").
Sample 1Sample 2
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“).
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 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").
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
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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. 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

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.

  • Ethical Standards ‌ 7.8.1 Within ninety (90) days after the Effective Date, Developer shall adopt written policies establishing ethical standards of conduct for all Developer-Related Entities, including Developer’s supervisory and management personnel, in dealing with (a) IFA and the Department and (b) employment relations. Such policy shall be subject to review and comment by IFA prior to adoption. Such policy shall include standards of ethical conduct concerning the following: 7.8.1.1 Restrictions on gifts and contributions to, and lobbying of, IFA, the Department and any of their respective members, commissioners, directors, officers and employees, and elected State officials; 7.8.1.2 Protection of employees from unethical practices in selection, use, hiring, compensation or other terms and conditions of employment, or in firing, promotion and termination of employees; 7.8.1.3 Protection of employees from retaliatory actions (including discharge, demotion, suspension, threat, harassment, pay reduction or other discrimination in the terms and conditions of employment) in response to reporting of illegal (including the making of a false claim), unethical or unsafe actions or failures to act by any Developer-Related Entity; 7.8.1.4 Restrictions on directors, members, officers or supervisory or management personnel of any Developer-Related Entity engaging in any transaction or activity, including receiving or offering a financial incentive, benefit, loan or other financial interest, that is, or to a reasonable person appears to be, in conflict with or incompatible with the proper discharge of duties or independence of judgment or action in the performance of duties, or adverse to the interests of the Project or employees; 7.8.1.5 Restrictions on use of office or job position for a purpose that is, or would to a reasonable person appear to be, primarily for the private benefit of a director, member, officer or supervisory or management person, rather than primarily for the benefit of Developer or the Project, or primarily to achieve a private gain or an exemption from duty or responsibility for a director, member, officer or supervisory or management person; and 7.8.1.6 Restrictions on directors, members, officers or employees of any Developer-Related Entity performing any of the Work if the performance of such services would be prohibited under IFA’s conflict of interest rules and policies. 7.8.2 Developer shall cause its directors, members, officers and supervisory and management personnel, and require those of all other Developer-Related Entities, to adhere to and enforce the adopted policy on ethical standards of conduct. Developer shall establish reasonable systems and procedures to promote and monitor compliance with the policy. 7.8.3 Notwithstanding the foregoing in this Section 7.8, Developer has an affirmative obligation under this Agreement to disclose to IFA and to the Indiana State Ethics Commission when an interested party is or becomes an employee of IFA or the State. This obligation extends only to those facts that Developer knows or reasonably could know. For purposes of this Section 7.8.3, “interested party” means (a) the individual executing this Agreement, (b) an individual who has an interest of three percent (3%) or more of Developer, (c) any member of the immediate family of an individual specified in clause (a) or (b). For purposes of the preceding sentence, “immediate family” means the spouse and the unemancipated children of an individual.‌

  • Content Standards You agree that you will not upload or provide content or otherwise post, transmit, distribute, or disseminate through the Zelle® Payment Service any material that: (1) is false, misleading, unlawful, obscene, indecent, lewd, pornographic, defamatory, libelous, threatening, harassing, hateful, abusive, or inflammatory; (2) encourages conduct that would be considered a criminal offense or gives rise to civil liability; (3) breaches or infringes any duty toward or rights of any person or entity, including rights of publicity, privacy or intellectual property; (4) contains corrupted data or any other harmful, disruptive, or destructive files; (5) advertises products or services competitive with Zelle®, as determined by Zelle® in its sole discretion; or (6) in Zelle®’s or our sole judgment, is objectionable, restricts or inhibits any person or entity from using or enjoying any portion of the Zelle® Payment Service, or which may expose us, Zelle® or our respective affiliates or customers to harm or liability of any nature.

  • 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.

  • Contractor Standards Contractor shall comply with Contractor Standards provisions codified in the SDMC. Contractor understands and agrees that violation of Contractor Standards may be considered a material breach of the Contract and may result in Contract termination, debarment, and other sanctions.

  • Security Standards The Provider shall implement and maintain commercially reasonable security procedures and practices that otherwise meet or exceed industry standards designed to protect Student Data from unauthorized access, destruction, use, modification, or disclosure, including but not limited to the unauthorized acquisition of computerized data that compromises the security, confidentiality, or integrity of the Student Data (a "Security Breach"). For purposes of the DPA and this Exhibit G, "Security Breach" does not include the good faith acquisition of Student Data by an employee or agent of the Provider or LEA for a legitimate educational or administrative purpose of the Provider or LEA, so long as the Student Data is used solely for purposes permitted by SOPPA and other applicable law, and so long as the Student Data is restricted from further unauthorized disclosure.

  • Work Standards The Contractor shall execute its responsibilities by following and applying at all times the highest professional and technical guidelines and standards. If the State becomes dissatisfied with the work product of or the working relationship with those individuals assigned to work on this Contract, the State may request in writing the replacement of any or all such individuals, and the Contractor shall grant such request.

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