Compass.ucsd.edu

Health Insurance Portability & Accountability Act HIPAA

A covered entity is an organization that, by virtue of providing healthcare services and billing for them using electronic means, is subject to the provisions of HIPAA. … See more

Actived: 8 days ago

URL: https://compass.ucsd.edu/health-insurance-portability-accountability-act-hipaa

What You Should Know Before Participating in a Research Study

WEBMedical research is an organized, well-planned study of a problem in health care. We engage in research to answer specific questions about what makes people sick and …

Category:  Medical Go Health

Good Clinical Practice Compass

WEBThe CITI Good Clinical Practice (GCP) Optional Modules Course is a 13-module program that discusses good clinical practice as it relates to clinical trials of both drugs/biologics …

Category:  Course Go Health

ClinicalTrials.Gov Compass

WEBThe US National Institutes of Health (NIH) final policy of 2016 established the expectation that all investigators conducting clinical trials funded in whole or in part by the NIH will …

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OCTA Office of Clinical Trials Administration Compass

WEBThe Office of Clinical Trials Administration (OCTA) has the responsibility and authority to negotiate and execute agreements that meet the above definition of a …

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Data & Safety Monitoring for Clinical Trials Compass

WEBThe NIH requires data and safety monitoring for all types of clinical trials, including physiologic, toxicity, and dose-finding studies (Phase I); efficacy studies …

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Epic EMR Compass

WEBContact Us. For immediate assistance, call x3HELP or. 619-543-4357. For general, non-urgent questions or feedback related to Epic: Click the button located on …

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Office of IRB Administration OIA Compass

WEBCriteria for IRB Approval. In order to evaluate and potentially approve human subjects research, the UC San Diego IRB must review the protocol and determine that …

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Data Management Compass

WEBData management plans (DMPs) encourage researchers to think about how they will responsibly handle the data they collect, and are required by many funders. The …

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Research Safety Compass

WEBSafety Reporting to the IRB. UCSD requires researchers to report any unanticipated problems involving risks to subjects or others in a timely manner. …

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CTA Clinical Trial Agreements Compass

WEBA clinical trial agreement is the contract between an industry sponsor and University outlining the obligations of each party for the conduct of a sponsor-authored …

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Training & Education Compass

WEBAll paid UC Health Sciences/Health Employees are required to complete this mandatory annual training. This training is designed to: 1) provide guidance on how to identify and …

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EPIC Electronic Medical Record (EMR) Compass

WEBAll users of UC San Diego Health Epic EMR must complete an assigned training curriculum that is customized for each employee based on their job and role. Training may be in the …

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Health Sciences Office of Compliance and Privacy Compass

WEBThe Office of Compliance and Privacy has been developed in the context of our core teaching, research, patient care, and public service missions.

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Investigational New Drug IND Compass

WEBPrepare the Initial IND Submission. The IND Sponsor-Investigator compiles information in three broad areas: Animal Pharmacology and Toxicology Studies: …

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Systems Compass

WEBIf you would like to reserve a space for a class, please send an email request to the CTRI Application Support Team at [email protected] and provide the name and date of the …

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Standard Operating Procedures SOPs Compass

WEBIn clinical research, SOPs help define the group’s (e.g., unit, division, department, institution, etc.) standard practices and daily processes conducted to assure …

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Consent Development Compass

WEBDocumentation of informed consent: Federal and state regulations direct that informed consent be documented, in general, with a written consent form approved in …

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