Researchgo

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Published on ResearchGo | UCLA (https://www.researchgo.ucla.edu) Study Applicable Fee effective 3/1/22 Non-Profit Funded Studies (including NIH) N/A Industry-Sponsored Studies $2,800 Industry-Sponsored Budget Amendments (per occurrence) $1,000Apr 13, 2023 · In addition, the FDA Affairs team has created a virtual clinical research platform called ResearchGo that provides a single portal to a wealth of resources, expertise, and best practices for investigators and research staff to facilitate efficient, compliant and ethical study conduct and management. Determination of product classification (e.g ... The NIH provides many resources for protocol development to assist investigators in writing and developing clinical research protocols that are in compliance with regulatory/GCP requirements. Some NIH institutes have a mandatory requirement for using their protocol template. Study Design consultation and assistance are available at UCLA.Published on ResearchGo | UCLA (https://www.researchgo.ucla.edu) Data Safety Monitoring Board (DSMB) Data Safety Monitoring Board (DSMB) A Data and Safety Monitoring Board (DSMB) is a group of individuals with pertinent expertise that reviews accumulating data from an ongoing clinical trial. The CTSI DSMB offers oversight for …Staff Resources. Our people, our power. Encouraging the talented members of our medical school staff to meet their life and career goals with determination and optimism.

CTSI ResearchGo. CTSI ResesarchGO is a clinical research portal to resources, expertise and best practices for investigators, study staff, and partners/affiliates. Information is available on study design, clinical study management, regulatory components, trainings and related CTSI services. Learn More About CTSI ResearchGoBy housing all patient information in one electronic database, it eliminates the duplication of tests, sends alerts to warn of allergies to medications or contradictions and creates an easily accessible mechanism for sharing information. Please call 310-267-2273 (7Care) to place a ServiceNow ticket for any assistance needed with ResearchConnect ...ResearchGo; UCLA CTSI; UCLA JCCC; Office of Human Subjects Protection; Search for Clinical Trials; Research Excellence. Breakthroughs; Funding Opportunities; Seminar Calendar; Support Science; Community and Equity Community and Equity sub-navigation. Justice, Equity, Diversity and Inclusion. JEDI Overview; Events; Communities; Data ...FIND RESEARCH OPPORTUNITIES ON THE UNDERGRADUATE RESEARCH PORTAL. You can find opportunities to do research in all disciplines through the Undergraduate Research Portal :. Search for research opportunities both on and off campusSep 14, 2023 · For Studies using CTRC Services. CTRC meetings are held every other Wednesday. A complete application and all requested documents must be received at [email protected] by 5pm the Wednesday prior to the scheduled CTRC Operations Committee meeting date. An incomplete submission may delay review. Need assistance or have clinical study ... ResearchGo. A platform with resources, expertise, and best practices for investigators, study staff, and partners/affiliates. See more about ResearchGo. K and R Grant Tips and Resources. Grant writing workshops, tips, and resources for residents, fellows, and junior faculty members. ...ResearchGo. A platform with resources, expertise, and best practices for investigators, study staff, and partners/affiliates. See more about ResearchGo. K and R Grant Tips and Resources. Grant writing workshops, tips, and resources for residents, fellows, and junior faculty members. ...Aug 26, 2022 · IRB Guidance for All Research Studies. Documentation of informed consent: Federal and state regulations direct that informed consent be documented, in general, with a written consent form approved in advance by the IRB and incorporating the required elements of consent. The participant or his/her legally authorized representative reads, signs ...

ResearchGo provides information, templates and resources to guide you through the IND process. An academic researcher may be required to submit an IND application to the FDA in order to study a marketed medical product in a new (i.e. unapproved) clinical indication. An investigator is always required to hold an IND to study anResearchGo; UCLA CTSI; UCLA JCCC; Office of Human Subjects Protection; Search for Clinical Trials; Research Excellence. Breakthroughs; Funding Opportunities; Seminar Calendar; Support Science; Community and Equity Community and Equity sub-navigation. Justice, Equity, Diversity and Inclusion. JEDI Overview; Events; Communities; Data ...The Office of Contracts and Grants Administration facilitates government and non-profit funding awards. For questions or assistance, please contact Patti Manheim, Director, Office of Contract and Grant Administration at (310) 794-2644. UCLA Technology Development Group (TDG) assists with industry supported basic and applied research, including ...The NIH provides many resources for protocol development to assist investigators in writing and developing clinical research protocols that are in compliance with regulatory/GCP requirements. Some NIH institutes have a mandatory requirement for using their protocol template. Study Design consultation and assistance are available at UCLA.

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The Device Accountability Log helps maintain study device inventory and can be included in the regulatory binder. Investigators are responsible for maintaining strict control over investigational drugs to ensure that the drug/biologic is used only for subjects enrolled in the study. The Drug or Biologic Dispensing/Accountability Log helps ...The document you are reading is not a static web page, but an interactive environment called a Colab notebook that lets you write and execute code. For example, ...EHR Trainings (ORCHID and i2b2 training offered by Liz Chen, Liz Chen, MBA, (310) 781-3601, [email protected]) Clinical Research Coordinators (SOCRA Chapter continuing education lectures; Clinical Research Coordinator Council) [email protected]. Good Clinical Practice (CITI) Ernestina Yiadom, 310-222-3624, [email protected] on ResearchGo | UCLA (https://www.researchgo.ucla.edu) Set-Up Research Budget The clinical research financial pulse provides a self service option for PI’s and study teams to create their own budgets using the current research pricing charge master. Study teams are best equipped to understand and validate researchPublished on ResearchGo | UCLA (https://www.researchgo.ucla.edu) Consent Development IRB Guidance for All Research Studies Formatting Guidelines for Consent Development Guidance, Tools and Templates Consent Development With few waivers and exceptions, researchers must obtain and document prospective consent from the …Aug 26, 2022 · The Clinical Research Coordinator Team (CRCT) carries through the compliant set-up of the clinical trial and oversees patient and study visit management, scheduling, and assists with general conduct of a clinical trial with PI oversight. Clinical Research Coordinator Services. Trained and credentialed clinical research coordinators that assist ...

Staff Resources. Our people, our power. Encouraging the talented members of our medical school staff to meet their life and career goals with determination and optimism.Community Partnered Research "How To" Series. "How To" documents are designed to help inform and guide community partners on a range of clinical research topics. Click on …Ancillary Research Services. Overview. Nuclear Medicine. Below and in the tabs at the right is information on the activities required relating to Ancillary services for you to activate your study. Note that your study activation could be delayed if you do not complete the study start up process required by the applicable Ancillary departments.IRB Guidance for All Research Studies. Documentation of informed consent: Federal and state regulations direct that informed consent be documented, in general, with a written consent form approved in advance by the IRB and incorporating the required elements of consent. The participant or his/her legally authorized representative reads, signs ...Last updated: 11 May 2023. Biostatistics UCLA offers a broad array of educational opportunities and biostat assistance in the methods of clinical research to meet the diverse needs of trainees, faculty and staff at UCLA. The UCLA CTSI Biostatistics, Epidemiology and Research Design Program provides integrated services and biostatistical support.Every year, DGSOM hosts a White Coat Ceremony for incoming first-year students. This ceremony caps off the Base Camp course, ushering students into their first year of medical school. The Service of Gratitude is an annual event held to honor, with sincere gratitude, the selfless legacy of the individuals who have donated their remains to DGSOM ...25 thg 6, 2022 ... Abstract: Research on water, energy, and food (WEF) is gradually becoming a global research hotspot in response to threats caused by the ...ResearchGo; Trial Innovation Network (TIN) DGIT Research Informatics Services. DGIT's Research Enablement Initiative brings together the UCLA Health IT teams to better understand researcher IT needs and to develop solutions that enhance research while minimizing disruptions and obstacles.ResearchGo provides information, templates and resources to guide you through the IND process. An academic researcher may be required to submit an IND …Community Partnered Research "How To" Series. "How To" documents are designed to help inform and guide community partners on a range of clinical research topics. Click on the links and thumbnails below to view and download the documents. Provides directions on designing a memorandum of understanding (MOU) which is a written agreement (not a ...National Institute of Dental and Craniofacial Research (NIDCR) - Study Tool: Study Close-out Checklist This document helps the investigator plan orderly closure of study documents, data, and publication. To close-out out a study on ClinicalTrials.Gov, please contact Elaine Cooperstein. For more information, please contact ResearchGo.

Published on ResearchGo | UCLA (https://www.researchgo.ucla.edu) Research Billing and Coding Health related services or procedures within a health system department that are provided as part of a clinical trial must be billed accurately. Accurate billing for research-related services is dependent on study documentation specificity.

Step 2. Win 10 Trainer Battles in the GO Battle League - x1000 Stardust. Win 20 Trainer Battles in the GO Battle League - x1000 Stardust. Win 30 Trainer Battles in the GO Battle League - x1000 ...Sep 14, 2023 · For Studies using CTRC Services. CTRC meetings are held every other Wednesday. A complete application and all requested documents must be received at [email protected] by 5pm the Wednesday prior to the scheduled CTRC Operations Committee meeting date. An incomplete submission may delay review. Need assistance or have clinical study ... Office of Regulatory Affairs. Description of Services. Scientific Review Committee. Data Safety Monitoring Board (DSMB) Internal Monitoring and Auditing. …See below for clinical trials contact information and the areas of research at: Cedars-Sinai. Charles R. Drew University of Medicine and Science. Lundquist/Harbor-UCLA. UCLA. Last updated: 15 Mar 2023. Overview Learn About Clinical Trials Clinical Translational Science Institute (CTSI) Community Information OHRPP Resources for Research ...Captivating English Research Paper Ideas. Effects of commercialization of sports. Dangers of consuming organic foods. The refugee crisis is increasing terrorism. Analysis of the Crisis between Ukraine and Russia. Impact of the controversial cartoon of Prophet Muhammad. The recent issue on Prophet Muhammad.Since 1976, the UCLA Jonsson Comprehensive Cancer Center has been designated a Comprehensive Cancer Center by the National Cancer Institute (NCI) of the National Institutes of Health (NIH). As such, the Cancer Center is dedicated to excellence and adherence to the highest ethical standards in both the delivery of patient care and the …Published on ResearchGo | UCLA (https://www.researchgo.ucla.edu) Research Billing and Coding Health related services or procedures within a health system department that are provided as part of a clinical trial must be billed accurately. Accurate billing for research-related services is dependent on study documentation specificity.Aug 26, 2022 · CITI Training Verification. UCLA OHRPP has created a CITI training lookup tool to search study team members and confirm any active and/or expired CITI trainings. Scroll down to the “CITI Training Lookup Tool” and click the hyperlink. Login with single sign on (either campus or mednet). You can search the individual name (s) of the study ...

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Mar 8, 2023 · REDCap - secure, web-based application for building and managing online surveys and data collection). UCLA CTSI offers complementary support during the process of defining and refining your database. UCLA Contact: Martin Lai, MS, (310) 794-9396, [email protected]. Harbor/LA Biomed Contact: Liz Chen, MBA, (310) 781-3601, [email protected]. Can Ethnographic Research Go Beyond the Status Quo? COURTNEY B. CAZDEN. Harvard Universib. This mticle is 17 slightly revised version of the Past President ...Contact ResearchGo. Group 1. Clinical Research Information Systems; UCLA Clinical Trials; Group 2. Office of Research Administration; Jonsson Comprehensive Cancer Center; Group 3. Office of Human Subjects Protection; CareConnect WebsiteKodaikanal Lake, the most popular tourist attraction in South India, is also contaminated. Kodaikanal mercury poisoning is a proven case of mercury contamination at the hill station of Kodaikanal, Tamil Nadu, India by Hindustan Unilever in the process of making mercury thermometers for export around the world. The exposé of the environmental …ResearchGo; UCLA CTSI; UCLA JCCC; Office of Human Subjects Protection; Search for Clinical Trials; Research Excellence. Breakthroughs; Funding Opportunities; Seminar Calendar; Support Science; Community and Equity Community and Equity sub-navigation. Justice, Equity, Diversity and Inclusion. JEDI Overview; Events; Communities; Data ...How Technological Developments Have Shaped and Evolved Healthcare. Medical technology advances in the last 50 years may have changed the practice of medicine, but they have also saved lives, increased access to care and improved quality of life. A brief look back to medicine in the 1960s may render a more realistic picture of the …ResearchGo; UCLA CTSI; UCLA JCCC; Office of Human Subjects Protection; Search for Clinical Trials; Research Excellence. Breakthroughs; Funding Opportunities; Seminar Calendar; Support Science; Community and Equity Community and Equity sub-navigation. Justice, Equity, Diversity and Inclusion. JEDI Overview; Events; Communities; Data ...Aug 26, 2022 · A Coverage Analysis is often associated with development of a billing grid, a tool which facilitates compliant clinical research billing, that distinguishes financial responsibility for study-related services between study funding and patients/insurers. UCLA Policy 915 requires Coverage Analysis be performed for any clinical research study ... See below for clinical trials contact information and the areas of research at: Cedars-Sinai. Charles R. Drew University of Medicine and Science. Lundquist/Harbor-UCLA. UCLA. Last updated: 15 Mar 2023. Overview Learn About Clinical Trials Clinical Translational Science Institute (CTSI) Community Information OHRPP Resources for Research ...Kenneth Lange, PhD. Professor, Human Genetics and Computational Medicine. [email protected]. His research interests include genetic epidemiology, population genetics, membrane physiology, demography, oncology, medical imaging, stochastic processes, and optimization theory. Many of his landmark papers predate by a decade or more the …The Department of Ophthalmology supports clinical research requiring ophthalmic procedures and testing for the UCLA community. While we have six clinical locations, we primarily provide ancillary services through our Stein Eye Institute and Doheny Eye Center locations. ….

If consent forms are maintained electronically or filed in the IRB section of the Binder, include a signed and dated note-to-file indicating the location. Once the IRB approves a new version of the consent form, the previous version expires. Previously approved versions can be kept in the IRB section of the Regulatory Binder.ResearchGo; UCLA CTSI; UCLA JCCC; Office of Human Subjects Protection; Search for Clinical Trials; Research Excellence. Breakthroughs; Funding Opportunities; Seminar Calendar; Support Science; Community and Equity Community and Equity sub-navigation. Justice, Equity, Diversity and Inclusion. JEDI Overview; Events; Communities; Data ...HOW DO I GET STARTED? Create an Online Research Profile. Login to the Undergraduate Research Portal using your UCLA logon.; On the upper right, under “Profiles,” select “Create/Update my Profile.”Published on ResearchGo | UCLA (https://www.researchgo.ucla.edu) IND Safety Report Cover Letter IND Safety Report and Instructions (not optimized for chrome) Safety Reporting Guidance Useful Links 21 CFR 312 Biological IND Submissions Center for Drug Evaluation & Research Guidance Documents (CDER)Clinical and Translational Research Centers (CTRCs) UCLA CTSI ResearchGo. Trial Innovation Network (TIN) Study coordinator services and. study activation. FDA/regulatory services. Funding opportunities and resources. More services for clinical research: Biostatistical consults and study design.ResearchGo. A platform with resources, expertise, and best practices for investigators, study staff, and partners/affiliates. See more about ResearchGo. K and R Grant Tips and Resources. Grant writing workshops, tips, and resources for residents, fellows, and junior faculty members. ...ResearchGO provides a single portal to resources, expertise, and best practices for investigators, study staff, and partners/affiliates. Design Study. Set Up Study.The Department of Ophthalmology supports clinical research requiring ophthalmic procedures and testing for the UCLA community. While we have six clinical locations, we primarily provide ancillary services through our Stein Eye Institute and Doheny Eye Center locations.Kenneth Lange, PhD. Professor, Human Genetics and Computational Medicine. [email protected]. His research interests include genetic epidemiology, population genetics, membrane physiology, demography, oncology, medical imaging, stochastic processes, and optimization theory. Many of his landmark papers predate by a decade or more the …Aug 26, 2022 · In clinical research, SOPs help define the group’s (e.g., unit, division, department, institution, etc.) standard practices and daily processes conducted to assure execution of research tasks in accordance with institutional, state and federal guidances. SOPs should contain adequate detail to clearly guide research staff through a particular ... Researchgo, Get a comprehensive Amazon data analysis from Go Global Agency to drive your e-commerce success. Our expert research team provides valuable insights on your ..., Last updated: 8 Mar 2023. About Us Researchers who require research imaging services for their industry-sponsored clinical/translational human studies apply through an electronic …, Nov 29, 2022 · Remote Monitoring FAQs. What is the Remote monitoring set up fee? For Industry (for profit) funded studies the cost is $2500 per study. The $2500 cost covers the provisioning of a study and one monitor for that study. For each additional monitor to be provisioned for that study, it is an additional $2000. Is the $2500 a one-time fee, or is it ... , Since 1976, the UCLA Jonsson Comprehensive Cancer Center has been designated a Comprehensive Cancer Center by the National Cancer Institute (NCI) of the National Institutes of Health (NIH). As such, the Cancer Center is dedicated to excellence and adherence to the highest ethical standards in both the delivery of patient care and the …, ResearchGO provides a single portal to resources, expertise, and best practices for investigators, study staff, and partners/affiliates. Design Study. Set Up Study., Aug 26, 2022 · The NIH requires data and safety monitoring for all types of clinical trials, including physiologic, toxicity, and dose-finding studies (phase I); efficacy studies (phase II); efficacy, effectiveness and comparative trials (phase III). Monitoring should be commensurate with risks. The method and degree of monitoring needed is related to the ... , Mar 8, 2023 · 21 CFR Part 11 outlines the federal requirements that help to ensure that electronic records are trustworthy, reliable, and generally equivalent to paper records and handwritten signatures executed on paper. If sponsors or the FDA have questions on Part 11 compliance of any UCLA Health Sciences systems or applications, researchers should ... , Turner-UCLA Allied Health Internship Program. The Turner UCLA Allied Health Internship is implemented by the UCLA Community Engagement Program, in partnership with Bobby and Lauren Turner, to provide learning opportunities for high school students and recent graduates in finding out more about careers in the entry-level, allied health professions., ResearchGo; UCLA CTSI; UCLA JCCC; Office of Human Subjects Protection; Search for Clinical Trials; Research Excellence. Breakthroughs; Funding Opportunities; Seminar Calendar; Support Science; Community and Equity Community and Equity sub-navigation. Justice, Equity, Diversity and Inclusion. JEDI Overview; Events; Communities; Data ..., In clinical research, SOPs help define the group’s (e.g., unit, division, department, institution, etc.) standard practices and daily processes conducted to assure execution of research tasks in accordance with institutional, state and federal guidances. SOPs should contain adequate detail to clearly guide research staff through a particular ..., Clinical and Translational Research Centers (CTRCs) UCLA CTSI ResearchGo. Trial Innovation Network (TIN) Study coordinator services and. study activation. FDA/regulatory services. Funding opportunities and resources. More services for clinical research: Biostatistical consults and study design., a computer vision researchGO. Home; Archives; github weibo google. 2016-12-27. 机器学习之数学基础 ML; Math. Math for Machine Learning author：Hal Daum e III. The goal of this document is to provide a “refresher” on continuous mathematics for computer science students. It is by no means a rigorous course on these topics., ResearchGo; Clinical and Translational Research Centers (CTRCs) Trial Innovation Network (TIN) Request a Service; Download Our Fliers; FAQs; Cite the Grant; Newsletter Sign Up; For the Public. Participate in a Clinical Trial; Clinical Research Centers; Jobs; FAQ; Site Map; Supported Browsers; Featured Projects., Mar 8, 2023 · This network focuses on breast cancer screening prevention studies, including the WISDOM study. WISDOM is a collaboration between all UCs and The Sanford Medical centers in the Midwest. To inquire about ECRI services, please contact ECRI director, Antonia Petruse at [email protected] or call office line at (310) 794-0367. , Shimon Weiss, DSC. Distinguished Professor, Chemistry and Biological Chemistry; Distinguished Professor, Physiology, Department of Physics, Institute for Nanotechnology and Advanced Materials, Bar-Ilan University Ramat-Gan, 52900 Israel. Transporters/ Channels/ Receptor / Biophysics. Fayal Abderemane-Ali, PhD. Assistant Professor, …, The Clinical Research Coordinator Team (CRCT) carries through the compliant set-up of the clinical trial and oversees patient and study visit management, scheduling, and assists with general conduct of a clinical trial with PI oversight. Clinical Research Coordinator Services. Trained and credentialed clinical research coordinators that assist ..., ResearchGO provides a single portal to resources, expertise, and best practices for investigators, study staff, and partners/affiliates. Learn more. Biomedical Library. Schedule a Virtual Research Consultation. Have a research question? Library staff are available to consult with you at every stage of the research process., Research Administration: Lundquist/Harbor UCLA: Allison Weber, Director Pre Award, Office of Research Administration. Office: (310)974-9567, Email: [email protected]. Compliance Office/Services: Lundquist/Harbor UCLA: For questions, contact Liz Burrola [email protected]. Conflicts of Interest :, Contact ResearchGo. Group 1. Clinical Research Information Systems; UCLA Clinical Trials; Group 2. Office of Research Administration; Jonsson Comprehensive Cancer Center; Group 3. Office of Human Subjects Protection; CareConnect Website, Aug 26, 2022 · Identify Funding Opportunities. Proposal Preparation and Submission. Data Management Planning. Set Up Research Budgets. Overview of Coverage Analysis. Billing Codes and Research Pricing Information. CTSI Integrating Special Populations Program (ISP) Request a CTSI Ethics Consultation. Last updated: 26 Aug 2022. , The Department of Ophthalmology supports clinical research requiring ophthalmic procedures and testing for the UCLA community. While we have six clinical locations, we primarily provide ancillary services through our Stein Eye Institute and Doheny Eye Center locations., Kodaikanal Lake, the most popular tourist attraction in South India, is also contaminated. Kodaikanal mercury poisoning is a proven case of mercury contamination at the hill station of Kodaikanal, Tamil Nadu, India by Hindustan Unilever in the process of making mercury thermometers for export around the world. The exposé of the environmental …, Per Monitoring Visit. Industry Funded Clinical Research Study. $2,500. $2,000. $1,000-$2,500. $250-$500. "Please note: all fees above are subject to the applicable UCLA indirect rate (s)." Remote monitoring set-up and provisioning fees may include, but are not limited to, facilitation of the following tasks: Remote monitoring terms and ... , 17 thg 10, 2018 ... Editors' Note: Collecting and analyzing three decades of NGO research, Allison Schnable, Jennifer N. Brass, and Rachel S. Robinson have ..., ResearchGo; Clinical and Translational Research Centers (CTRCs) Trial Innovation Network (TIN) Request a Service; Download Our Fliers; FAQs; Cite the Grant; Newsletter Sign Up; For the Public. Participate in a Clinical Trial; Clinical Research Centers; Jobs; FAQ; Site Map; Supported Browsers; Featured Projects., The CTSI provides the research infrastructure to translate discoveries to improve health in Los Angeles County, a diverse metropolis of 10 million people. Our institutions and affiliates encompass a range of health care delivery systems and research environments that include academic medical centers, safety-net hospitals and community clinics., Human Subjects / IRB Process. All UCLA key personnel conducting human research are required to complete human subjects protection training through an online program called the Collaborative Institutional Training Initiative (CITI). webIRB is UCLA's internet-based software application for the submission and review of research projects …, Aug 26, 2022 · In clinical research, SOPs help define the group’s (e.g., unit, division, department, institution, etc.) standard practices and daily processes conducted to assure execution of research tasks in accordance with institutional, state and federal guidances. SOPs should contain adequate detail to clearly guide research staff through a particular ... , Device study Coverage Requirements Investigators participating in an Investigational Device Exemption (IDE) Study that plans to request reimbursement for study procedures and materials from Medicare or third-party payers must ensure the following: CMS IDE study coverage has been approved by CMS or local Medicare contractor CMS approval of …, Aug 26, 2022 · Description of Services. The Office of Regulatory Affairs (ORA) provides a broad spectrum of support for Clinical Investigators and their study teams in the conduct and navigation of clinical research regulatory requirements. Services provided by this office include: Scientific and Feasibility Review, Data and Safety Monitoring, internal ... , Mar 8, 2023 · LA Biomed/Harbor-UCLA Medical Center: Information Systems & Technology, Director, Mark Sleet (310) 222-6519 [email protected]. Charles R. Drew University of Medicine and Science: not applicable at this time. Data Management Guidance including Tools, Resources and Data Storage options. , The Device Accountability Log helps maintain study device inventory and can be included in the regulatory binder. Investigators are responsible for maintaining strict control over investigational drugs to ensure that the drug/biologic is used only for subjects enrolled in the study. The Drug or Biologic Dispensing/Accountability Log helps ..., National Institute of Dental and Craniofacial Research (NIDCR) - Study Tool: Study Close-out Checklist This document helps the investigator plan orderly closure of study documents, data, and publication. To close-out out a study on ClinicalTrials.Gov, please contact Elaine Cooperstein. For more information, please contact ResearchGo.