Researchgo.ucla.edu

Access Electronic Health Records ResearchGo UCLA

WebIf needed, Informatics collaborates with the Biostatistics Program to integrate electronic health record (EHR) data with other kinds of data and analytic efforts. Informatics also …

Actived: 4 days ago

URL: https://www.researchgo.ucla.edu/access-electronic-health-records

Data & Safety Monitoring for Clinical Trials ResearchGo UCLA

WebThe 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); …

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ClinicalTrials.Gov ResearchGo UCLA

WebThe US National Institutes of Health (NIH) Policy on the Dissemination of NIH-Funded Clinical Trial Information of 2016 establishes the expectation that all NIH-funded …

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Guidance, Tools and Templates ResearchGo UCLA

WebIRB Guidance for All Research Studies. Documentation of informed consent: Federal and state regulations direct that informed consent be documented, in general, with a written …

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Applicable Clinical Trials ResearchGo UCLA

WebApplicable Clinical Trials [accordion collapsed] Definition of a Clinical Trial The World Health Organization (WHO) defines a clinical trial as “any research study that prospectively …

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Office of Regulatory Affairs ResearchGo UCLA

WebDescription 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 …

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Remote and On-Site Monitoring FAQs ResearchGo UCLA

WebFor Industry (for profit) funded studies the cost is $3000 per study. The $3000 cost covers the provisioning of a study and one monitor for that study. For each additional monitor to …

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What is 21 CFR Part 11

WebWhat is 21 CFR Part 11? 21 CFR Part 11 outlines the federal requirements that help to ensure that electronic records are trustworthy, reliable, and generally equivalent to paper …

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CareConnect/Research Connect ResearchGo UCLA

WebWhat is CareConnect? (overall Epic) CareConnect is UCLA's electronic health record (EHR) program, which integrates inpatient and outpatient clinical records with appointments, …

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Sponsor Monitoring and Auditing for Clinical Research Studies

WebSponsor Monitoring and Auditing for Clinical Research Studies For clinical research studies where a study sponsor is obligated by the FDA to monitor study source records, …

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Biostatistics ResearchGo UCLA

WebPhone: 310-248-8901, fax: 310-423-4020. Office: Pacific Theatres Building, 116 North Robertson Blvd. Suite 900C, Los Angeles, CA 90048. Last updated: 1 Feb 2024. …

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Coverage Analysis ResearchGo UCLA

WebCoverage Analysis (CA) is a financial review of a Clinical Research Study that is required to be performed pursuant to the Federal Clinical Trials Policy (also known as the National …

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Investigator Support Services

WebServices provided by this office include: Scientific and Feasibility Review, Data and Safety Monitoring, internal monitoring and auditing support, FDA and Sponsor inspection/audit …

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COVID-19 Information ResearchGo UCLA

WebThe CTSI Clinical Research COVID-19 help desk mailbox is now live. The purpose of the mailbox is to help capture and facilitate inquiries related to conducting COVID-19 …

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HIPAA Information & Training ResearchGo UCLA

WebAll faculty, staff, house staff, students, contractors and volunteers will be expected to complete the HIPPA Education and Training Program module and test. This includes …

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Embedded Clinical Research and Innovation Unit (ECRI)

WebThis 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 …

Category:  Cancer,  Medical Go Health

Integrating Special Populations (ISP) ResearchGo UCLA

WebISP Services The CTSI Integrating Special Populations Program (ISP) increases the quantity and quality of research in children, older adults, and populations affected by …

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UCLA Clinical Research External Monitoring & Auditing Policy …

WebIII. POLICY STATEMENT. UCLA is committed to supporting clinical research monitoring and auditing while maintaining the privacy and con]dentiality of research participants and in …

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