Research Procedures Sample Clauses

Research Procedures. The Company shall conduct the Sponsored Research in good scientific manner, and in compliance in all material respects with all requirements of applicable laws and regulations and alt applicable good laboratory practices. The parties recognize that the Sponsored Research is of an early-stage, developmental nature and that the Company hereby disclaims all representations and warranties, express and implied, that the Sponsored Research will be successfully completed, achieve any particular result, objective or outcome or be completed, or reach any particular stage or point of development, within the Research Period.
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Research Procedures. EHBE shall conduct the Project in good scientific manner, and in compliance with all applicable Collaborator policies and procedures as detailed in the applicable Project Plan, all requirements of applicable laws and regulations, the highest professional industry standards and good laboratory and/or clinical practices, including, without limitation, any quality assurance, quality control and other standards set forth in the applicable Project Plan. EHBE shall proceed diligently with the work set out in the applicable Project Plan for such Project, including, without limitation, by allocating sufficient time and effort and using personnel with sufficient skills and experience, together with sufficient equipment and facilities, to conduct such Project and to accomplish the goals set out therein.
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Research Procedures. 6 2.1.1 Immune Response Manufacture...................... 7 2.1.2 Conduct of Research.............................. 7 2.1.3
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Research Procedures. The Research Program is described more specifically in Exhibit B, which, along with any amendments thereto approved by the Steering Committee, is incorporated herein by reference. Generally, Immune Response shall optimize its [CONFIDENTIAL TREATMENT REQUESTED] by construction and improvement of plasmid vectors to obtain the required level and duration of Factor VIII expression from the recombinant Factor VIII constructs provided by Bayer. The optimization may be multi staged, for example, an initial optimization to reach the requisite level and duration of expression for the purposes of reaching Milestone 6.2.1 and further optimization to reach the requisite product profile for the purposes of reaching Milestone 6.2.3. [CONFIDENTIAL TREATMENT REQUESTED] Bayer will assist Immune Response in the construction and improvement of plasmid vectors and will
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Research Procedures. ‌ Research was conducted over a 70-day period between May and August 2010 in the Indian states of New Delhi and Bihar. Secondary data collection and planning for field research in Bihar took place in New Delhi from May 28 until June 30 with the assistance of Dr. Xxxxxx Xxx, a Consultant and expert in nutrition, and Xxxxxxx Xxxxxxxxxx, a member of the India study team and a faculty member of the Population Health Foundation of India. Field research was conducted in Bihar between July 1 and August 9 of which 30 days were spent in Patna and 10 days were spent in Nalanda and West Champaran Districts. UNICEF’s Senior Nutrition Advisor, Xx. Xxxxxx Xxxxxx, facilitated a meeting with the Chief Secretary of the Government of Bihar to obtain official support for conducting research in Bihar. At the Chief Secretary’s request, the Development Commissioner for the Government of Bihar convened a meeting on 26 July for the study’s Principal Investigator, Primary Investigator for India and myself to meet with representatives of key government departments and programs (NRHM, Social Welfare, Public Health Engineering, and Rural Development) in order to discuss the project and initiatives by the Government of Bihar to reduce maternal undernutrition and improve birth outcomes. Secondary data were collected throughout the study period on the magnitude and distribution of malnutrition and its determinants and the coverage, intensity, and quality of interventions and services to improve the nutritional status of adolescent girls and women, and potential alternative platforms for delivering interventions and services to improve the nutritional status of adolescent girls and women. Secondary data sources included representative, population-based survey reports (e.g. National Family Health Surveys and District Level Health Surveys), program planning documents (e.g. NRHM Program Implementation Plan 2010-2011), first- and third- party program evaluations, technical guidelines, annual reports, journal articles, news stories, and organizational
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Research Procedures. Should you decide to allow your child to participate in this research study, you will be asked to sign this consent form once all your questions have been answered to your satisfaction. The children will use the learning platform which shows playful content the teachers have created by themselves beforehand. The gameful experience may include a location-based game, which may track GPS data of the used device during gameplay in order for the game to work correctly. After using the software a survey will be administered via the participating teachers based on their engagement with the individual students interacting with the learning platform. The teachers will be asked to provide answers to a series of questions related to the student’s experience of using the learning platform. Risks The investigators perceive no risks from your child’s involvement in this study (that is, no risks beyond the risks associated with everyday life). Payment for participation There will be no incentives or rewards in this study. Participation & Withdrawal Your child’s participation is entirely voluntary. He/she is free to choose not to participate. Should you and your child choose to participate, he/she can withdraw at any time without consequences of any kind. Questions about the Study If you have questions or concerns during the time of your child’s participation in this study, or after its completion or you would like to receive a copy of the final aggregate results of this study, please contact: [CONTACT DETAILS] #2018P01 Data Privacy Statement Authority: [PARTNER NAME, Conductor, Address, email address, Telephone number] is in charge of the data collection and processing of this workshop. Xxxxxxxxx Xxxxx, Coventry University Priory Street, Coventry, United Kingdom, CV1 5FB xx0000@xxxxxxxx.xx.xx is the project coordinator of BEACONING. BEACONING is a European funded project in which 15 partners in 9 countries (United Kingdom, Germany, Portugal, Spain, France, Romania, Italy, Poland and Turkey) are working closely together. All partners are listed here: xxxx://xxxxxxxxx.xx/insights/the- who/ Voluntary information: While you use the BEACONING platform, we only collect data that is needed by the system in order to work properly. You will receive [questionnaires and a feedback form] we kindly ask you to fill in. These are not mandatory and there are no negative consequences if these are not be filled in. Data processing:
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Research Procedures. VivaCell shall conduct the Project in good scientific manner, and in compliance with all applicable Collaborator policies and procedures as detailed in the applicable Project Plan, all requirements of applicable laws and regulations, the highest professional industry standards and good laboratory and/or clinical practices, including, without limitation, any quality assurance, quality control and other standards set forth in the applicable Project Plan. VivaCell shall proceed diligently with the work set out in the applicable Project Plan for such Project, including, without limitation, by allocating sufficient time and effort and using personnel with sufficient skills and experience, together with sufficient equipment and facilities, to conduct such Project and to accomplish the goals set out therein.
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Research Procedures. The information from teachers and directors as well as the primary school students was collected using trained field team members, utilizing IDI guides as well as FGD facilitation guides. The data were collected, transcribed, analyzed, and used to make programmatic recommendations for program improvement.
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Research Procedures 
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Related to Research Procedures

  • New Procedures New procedures as to who shall provide certain of these services in Section 1 may be established in writing from time to time by agreement between the Fund and the Transfer Agent. The Transfer Agent may at times perform only a portion of these services and the Fund or its agent may perform these services on the Fund's behalf;

  • DISCIPLINE PROCEDURES The discipline procedure may be initiated only within twenty (20) Days of the date the President or Vice-President (Academic and Research) knew, or ought reasonably to have known, of the occurrence of the matter giving rise to discipline. The Employer shall have the right to request, in writing to the Union, an extension of ten (10) Days. The Union shall not unreasonably reject the Employer’s request.

  • AML/KYC Procedures “AML/KYC Procedures” means the customer due diligence (CDD) procedures of a Reporting Financial Institution pursuant to the anti-money laundering or similar requirements of the jurisdiction concerned to which such Reporting Financial Institution is subject.

  • Evaluation Procedures 7.2.1 Evaluation procedures designed to fairly and adequately assess performance of full- time faculty employees shall be established and reviewed annually by the Vice President, after consultation with appropriate faculty groups at divisional/departmental meetings for their recommendations.

  • NEGOTIATIONS PROCEDURES Section 1. Negotiations shall commence pursuant to Article 4 of this Agreement and the Parties will structure their Agreement per the four (4) Agency groups set forth below: HUMAN SERVICES: Department of Human Services-Oregon Health Authority, Employment Department; INSTITUTIONS: Oregon Youth Authority (Youth Correctional Facilities), Oregon Health Authority Institutions: Oregon State Hospital (OSH), Pendleton State-Delivered Secure Residential Treatment Facility (Pendleton Cottage), OYA Administration and Field Services; ODOT: Oregon Department of Transportation (ODOT), Forestry, Oregon Parks and Recreation Department (OPRD), Oregon Department of Aviation (ODOA), Oregon Department of Fish & Wildlife (ODFW), Department of Geology and Mineral Industries (DOGAMI), Department of Agriculture, Water Resources Department, Oregon Watershed Enhancement Board; SPECIAL AGENCIES: Justice, Revenue, Higher Education Coordinating Commission, Workers’ Compensation Board, Department of Consumer & Business Services (DCBS), Bureau of Labor and Industries (BOLI), Veterans’ Affairs, Board of Nursing, Oregon Medical Board, Board of Dentistry, Board of Pharmacy, Mortuary and Cemetery Board, Oregon Mental Health Regulatory Agency, Board of Medical Imaging, Board of Massage Therapists, Occupational Therapy Licensing Board, Board of Examiners for Speech Pathology & Audiology, Board of Naturopathic Medicine, Education, Library, Treasury, Commission for the Blind, Public Employees Retirement System (PERS), Special Schools, State Scholarship, Department of Administrative Services, Oregon Housing & Community Services (OHCS), Oregon State Board of Examiners for Engineering and Land Surveying (OSBEELS), and Teachers Standards and Practices Commission.

  • Testing Procedures Testing will be conducted by an outside certified Agency in such a way to ensure maximum accuracy and reliability by using the techniques, chain of custody procedures, equipment and laboratory facilities which have been approved by the U.S. Department of Health and Human Services. All employees notified of a positive controlled substance or alcohol test result may request an independent test of their split sample at the employee’s expense. If the test result is negative the Employer will reimburse the employee for the cost of the split sample test.

  • Medical Procedures The Board shall distribute a copy of its Operating Procedures for administration of prescribed medication to pupils in schools and procedures for health support services to each Continuing Education Teacher.

  • Research Use Reporting To assure adherence to NIH GDS Policy, the PI agrees to provide annual Progress Updates as part of the annual Project Renewal or Project Close-out processes, prior to the expiration of the one (1) year data access period. The PI who is seeking Renewal or Close-out of a project agree to complete the appropriate online forms and provide specific information such as how the data have been used, including publications or presentations that resulted from the use of the requested dataset(s), a summary of any plans for future research use (if the PI is seeking renewal), any violations of the terms of access described within this Agreement and the implemented remediation, and information on any downstream intellectual property generated from the data. The PI also may include general comments regarding suggestions for improving the data access process in general. Information provided in the progress updates helps NIH evaluate program activities and may be considered by the NIH GDS governance committees as part of NIH’s effort to provide ongoing stewardship of data sharing activities subject to the NIH GDS Policy.

  • Review Procedures The Parties agree to jointly conduct a review, sampling transactions of the incidents managed under this Agreement. Findings that are inconsistent with the normal or accepted way of doing business will be reconciled on a case by case basis. Any decision to further examine records will be considered on a case by case basis and appropriate follow up action agreed upon by all agencies involved.

  • SAFETY PROCEDURES The Contractor shall:

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