Good Clinical Practices (GCP)

Good Clinical Practices (GCP) is an international quality standard that governs the ethical and scientific conduct of clinical trials involving human subjects. Coursera's Good Clinical Practices (GCP) catalogue teaches you the fundamental principles and guidelines established by the International Council for Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH). You'll learn to implement rigorous protocols, ensure participant safety, maintain comprehensive documentation, and adhere to ethical standards in clinical research. Mastering GCP is essential for professionals in the pharmaceutical and healthcare industries, enabling them to conduct high-quality clinical trials that meet regulatory requirements and contribute to the development of safe and effective medical treatments.
3credentials
8courses

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Results for "good clinical practices (gcp)"

  • Status: Free Trial

    Skills you'll gain: Good Clinical Practices (GCP), Informed Consent, Institutional Review Board (IRB), Clinical Research Ethics, Clinical Research Coordination, Clinical Research, Clinical Trials, Clinical Data Management, Drug Development, Patient Education And Counseling, Record Keeping, Clinical Documentation, Regulatory Compliance, Document Management, Health Equity, Electronic Medical Record, Patient Communication, Risk Management

  • Status: Free Trial

    Johns Hopkins University

    Skills you'll gain: Clinical Data Management, Clinical Trials, Sample Size Determination, Clinical Research Ethics, Clinical Trial Management Systems, Clinical Research, Data Quality, Quality Assurance, Data Entry, Case Report Forms, Institutional Review Board (IRB), Good Clinical Practices (GCP), Data Cleansing, Data Management, Regulatory Compliance, Data Integrity, Statistical Reporting, Informed Consent, Clinical Documentation, Data Collection

  • Status: Free Trial

    Skills you'll gain: Good Clinical Practices (GCP), Clinical Research, Clinical Trials, Clinical Research Ethics, Informed Consent, Clinical Data Management, Institutional Review Board (IRB), Patient Education And Counseling, Drug Development, Health Equity, Risk Management

  • Status: Free Trial

    Skills you'll gain: Good Clinical Practices (GCP), Informed Consent, Clinical Research, Clinical Trials, Clinical Research Ethics, Institutional Review Board (IRB), Drug Development, Record Keeping, Clinical Documentation, Regulatory Compliance, Patient Communication

  • Status: Preview

    Skills you'll gain: Clinical Data Management, Electronic Data Capture (EDC), Data Management, Data Collection, Case Report Forms, Data Sharing, Health Informatics, Data Strategy, Data Quality, Good Clinical Practices (GCP), Sampling (Statistics), Data Integrity, Data Validation, Regulatory Compliance

  • Status: Free Trial

    Skills you'll gain: Good Clinical Practices (GCP), Institutional Review Board (IRB), Clinical Research Ethics, Clinical Research Coordination, Clinical Trials, Clinical Research, Drug Development, Informed Consent, Document Management, Electronic Medical Record

What brings you to Coursera today?

  • Status: Free Trial

    Johns Hopkins University

    Skills you'll gain: Clinical Trials, Clinical Research, Clinical Research Ethics, Good Clinical Practices (GCP), Informed Consent, Biostatistics, Healthcare Ethics, Science and Research, Regulatory Compliance

  • Status: Free Trial

    Skills you'll gain: Clinical Research Ethics, Clinical Trial Management Systems, Clinical Trials, Clinical Research, Good Clinical Practices (GCP), Institutional Review Board (IRB), Regulatory Compliance, Clinical Documentation, Scientific Methods, Record Keeping

  • Status: Free Trial

    University of Michigan

    Skills you'll gain: Institutional Review Board (IRB), Clinical Trials, Health Policy, Health Disparities, Clinical Research, Clinical Research Ethics, Health Equity, Healthcare Ethics, Public Health, Epidemiology, Good Clinical Practices (GCP), Pre-Clinical Development, Policty Analysis, Research, and Development, Health Care, Medical Science and Research, Policy Development, Health Care Procedure and Regulation, Community Health, Drug Development, Research

  • Status: Preview

    Skills you'll gain: Pharmaceuticals, Clinical Trials, Drug Development, Clinical Research Ethics, Healthcare Ethics, Good Clinical Practices (GCP), Pharmacology, Regulatory Affairs, Healthcare Industry Knowledge, Emerging Technologies, Regulatory Compliance, Precision Medicine, Biotechnology

  • Status: Free Trial

    University of Michigan

    Skills you'll gain: Institutional Review Board (IRB), Clinical Trials, Clinical Research, Clinical Research Ethics, Healthcare Ethics, Good Clinical Practices (GCP), Medical Science and Research, Drug Development, Research, Health Policy, Pharmaceuticals, Patient Safety