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  • Good Clinical Practice
    The Good Clinical Practice (GCP) course is designed to prepare research staff in the conduct of clinical trials with human participants The 12 modules included in the course are based on ICH GCP Principles and the Code of Federal Regulations (CFR) for clinical research trials in the U S The course is self-paced and takes approximately six hours to complete To preview the new enhanced
  • Good Clinical Practice
    Please enter your first and last name as you would like it to appear on your certificate You will NOT be able to change your name later
  • Good Clinical Practice
    This training has been funded in whole or in part with Federal funds from the National Institute on Drug Abuse, National Institutes of Health, Department of Health and Human Services, under Contract No 75N95024D00037
  • Good Clinical Practice
    About In collaboration with the National Institute on Drug Abuse (NIDA) Center for Clinical Trials (CCTN) Clinical Trials Network (CTN) this Good Clinical Practice (GCP) online training was developed to prepare study staff responsible for the conduct of trials with human participants from protocol development through study closeout
  • Good Clinical Practice
    Wondering what's different in the redesign? The new GCP website offers a number of enhancements for our users to enjoy: Recent modifications made to the ICH GCP guidelines, which have been incorporated into the instructional material Highly engaging and relevant e-learning interactions have been incorporated throughout the course to improve the learner's ability to understand and retain the
  • Overview of Good Clinical Practice Training
    Overview of Good Clinical Practice Training The Good Clinical Practice (GCP) online training consists of 12 modules Each module discusses a specific GCP standard General conduct of research standards are also presented
  • Good Clinical Practice
    This training course is based on International Conference on Harmonization (ICH) Guidelines as best practices and regulatory requirements for conducting clinical research trials in the United States While the scenarios discussed are related to substance abuse treatment, the concepts are applicable to all clinical research
  • Good Clinical Practice
    NIDA CCTN Clinical Trials Network CTN Dissemination Library Network Updates Training Sessions and Webinars ClinicalTrials gov NIH Certificates of Confidentiality Kiosk Training on Protecting Human Research Participants U S DHHS Office of Human Research Protections (OHRP) Federalwide Assurance (FWA) U S DOJ Drug Enforcement Administration (DEA)
  • Good Clinical Practice - gcp. nidatraining. org
    IRB review of incentives for clinical research participation IRBs and confidentiality Individually Identifiable Health Information Information that should be documented in both clinical and research progress notes Information to be included in the consent document Informed Consent of Trial Participants Institutional Review Boards





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