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The New Era of Clinical Trials: Adopting Electronic Informed Consent

HIT Consultant

Director, Product & Strategy, Patient Consent, IQVIA Technologies The clinical trials landscape continues to evolve and with it, an exponential growth in the adoption of electronic informed consent (eConsent) solutions. About Vinita Navadgi Vinita Navadgi is the Sr.

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CMS Releases New Guidance Regarding Informed Consent for Sensitive Exams

Hall Render

Department of Health and Human Services (“HHS”), through the Centers for Medicare & Medicaid Services (“CMS”) released a memorandum to state survey agency directors highlighting revisions and clarification to the Hospital Interpretive Guidelines for Informed Consent (the “Guidance”).

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Informed Consent in Healthcare Training

American Medical Compliance

When a medical professional informs a patient of the advantages, disadvantages, and alternatives of a procedure or intervention, informed consent is obtained. According to the Joint Commission, all aspects of informed consent must be documented “in a form, progress notes, or elsewhere in the record.”

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Quality Data Leads to Better Outcomes, Alignment & Informed Consent at ViVE2023

Healthcare IT Today

We caught up with XSOLIS Co-founder Jim Sohr to learn more about the company. Measuring Data Quality – Clinical Architecture We talk a lot about needing good quality data in order to run analytics or train AI algorithms, but what does that really mean? Be sure to check all our coverage of the ViVE conference.

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FDA Finalizes Its Informed Consent Guidance for IRBs, Clinical Investigators and Sponsors

Hall Render

Food and Drug Administration (“FDA”) finalized “ Informed Consent: Guidance for IRBs, Clinical Investigators, and Sponsors ” (“Final Guidance”), following the FDA’s earlier issuance of draft guidance on the subject in July 2014. Informed consent includes the following basic elements: Description of clinical investigation.

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Adding COVID-19 to the informed consent process: A Q&A for health care providers

Health Law Checkup

To minimize their risk should a patient be exposed to COVID-19 while seeking medical care, health care providers should consider supplementing their informed consent process to include information about COVID-19 risks.

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Why We Should Care About the Move from Saliva to Living Cells in Precision Medicine

Bill of Health

A “yourtissueandyou” would be decidedly more informative — but also more invasive — than a 23andMe. With living cells, the types and volume of information one can obtain about a patient are more varied and greater than what can be obtained from saliva.

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