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.
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.
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.
Research Procedures. 6 2.1.1 Immune Response Manufacture...................... 7 2.1.2 Conduct of Research.............................. 7 2.1.3
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.
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. The investigators perceive no risks from your child’s involvement in this study (that is, no risks beyond the risks associated with everyday life). There will be no incentives or rewards in this study. 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. 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 Authority: [PARTNER NAME, Conductor, Address, email address, Telephone number] is in charge of the data collection and processing of this workshop. ▇▇▇▇▇▇▇▇▇ ▇▇▇▇▇, Coventry University Priory Street, Coventry, United Kingdom, CV1 5FB ▇▇▇▇▇▇@▇▇▇▇▇▇▇▇.▇▇.▇▇ 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: ▇▇▇▇://▇▇▇▇▇▇▇▇▇.▇▇/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:
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.
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. ▇▇▇▇▇▇ ▇▇▇, a Consultant and expert in nutrition, and ▇▇▇▇▇▇▇ ▇▇▇▇▇▇▇▇▇▇, 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, ▇▇. ▇▇▇▇▇▇ ▇▇▇▇▇▇, 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
Research Procedures