Informed Consent

Informed Consent is a critical ethical and legal principle in healthcare and research that ensures individuals have sufficient information to make autonomous decisions about their medical care or participation in studies. Coursera's Informed Consent catalogue teaches you the fundamental components of this process, including disclosure of relevant information, assessment of patient comprehension, and voluntary agreement. You'll learn to effectively communicate risks and benefits, respect patient autonomy, document consent properly, and navigate complex scenarios involving vulnerable populations or emergency situations. Mastering Informed Consent empowers healthcare professionals and researchers to uphold ethical standards, protect patient rights, and foster trust in medical and scientific practices, ultimately leading to better patient outcomes and more responsible research conduct.
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Results for "informed consent"

  • Status: Free Trial

    University of Pennsylvania

    Skills you'll gain: Health Care Procedure and Regulation, Medicaid, Healthcare Industry Knowledge, Medicare, Managed Care, Health Care Administration, Law, Regulation, and Compliance, Healthcare Ethics, Health Policy, Legal Risk, Lawsuits, Informed Consent, Case Law, Emergency Departments

    4.9
    Rating, 4.9 out of 5 stars
    261 reviews

    Beginner · Course · 1 - 4 Weeks

  • Status: Preview

    University of Maryland, College Park

    Skills you'll gain: Data Integration, Data Ethics, R Programming, Surveys, Informed Consent, Statistical Methods, Statistical Analysis, Sampling (Statistics), Regression Analysis, Statistical Modeling, Descriptive Statistics

    Mixed · Course · 1 - 4 Weeks

  • Status: Preview

    Fred Hutchinson Cancer Center

    Skills you'll gain: Responsible AI, ChatGPT, Data Ethics, Generative AI, Social Justice, Artificial Intelligence, Ethical Standards And Conduct, Data Validation, Informed Consent, Verification And Validation, Diversity and Inclusion, Mitigation, Algorithms, Data Science

    5
    Rating, 5 out of 5 stars
    7 reviews

    Beginner · Course · 1 - 4 Weeks

  • Packt

    Skills you'll gain: Clinical Trials, Clinical Data Management, Clinical Research, Case Report Forms, SAS (Software), Statistical Reporting, Pharmaceuticals, Data Analysis, Statistical Analysis, Informed Consent, Data Manipulation, Descriptive Statistics

    Beginner · Course · 1 - 4 Weeks

  • Status: Free Trial

    University of Maryland, College Park

    Skills you'll gain: Statistical Analysis, STATA (Software), R (Software), Data Integration, Data Ethics, Stata, R Programming, Sampling (Statistics), Statistical Modeling, Descriptive Statistics, Regression Analysis, Informed Consent, Information Privacy

    4.1
    Rating, 4.1 out of 5 stars
    64 reviews

    Mixed · Course · 1 - 4 Weeks

  • Status: Free Trial

    Coursera Instructor Network

    Skills you'll gain: Data Ethics, Business Ethics, Ethical Standards And Conduct, Responsible AI, Artificial Intelligence, Information Privacy, Informed Consent, Personally Identifiable Information, Accountability, Generative AI Agents, Data Governance, Data Collection, Algorithms

    Beginner · Course · 1 - 4 Weeks

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Leading partners

  • Novartis
  • Johns Hopkins University
  • Fred Hutchinson Cancer Center
  • MedCerts
  • Packt
  • Pontificia Universidad Católica del Perú
  • University of Cape Town
  • University of Maryland, College Park