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.
Overview of Good Clinical Practice Training - gcp.nidatraining.org
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 - gcp.nidatraining.org
The material is based on US CFR, International GCP guidelines, and human subject protection requirements for conducting clinical research. While this program is available to study staff participating in the NIDA Clinical Trials Network, the training is open-access to the public.
Good Clinical Practice - gcp.nidatraining.org
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 ...
Good Clinical Practice - gcp.nidatraining.org
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. HHSN27201201000024C.
Good Clinical Practice - gcp.nidatraining.org
2017年3月3日 · 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 - gcp.nidatraining.org
The Good Clinical Practice (GCP) guidelines of the International Council for Harmonization (ICH) define an adverse event (AE) as “any untoward medical occurrence in a patient or clinical investigation subject administered a pharmaceutical product and that does not necessarily have a causal relationship with this treatment.”
Good Clinical Practice - gcp.nidatraining.org
Clinical Trials Network. Good Clinical Practice. About; Contact Us; Toggle navigation. Welcome. Resources. FAQs. Create an Account. 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. First Name *