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 …

The course is designed to be comprehensive for users to review the content of required information in conjunction with an examination of other source documents and websites pertinent to Good Clinical …

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 …

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 …

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. …

Network Updates Training Sessions and Webinars ClinicalTrials.gov NIDA Clinical Coordinating Center NIH Certificates of Confidentiality Kiosk (For non-IND studies) NIH Training on Protecting Human …

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.

Mar 3, 2017 · 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 …

Exceptions Exceptions to requirement for children's assent Exceptions to requirement to obtain parental permission Good Clinical Practice Summary Good medical record practices to observe when writing …

Selection of Expert Trainers 10.3.3.1. Training the Trainer and Supervisors 10.3.3.2. Credentialing of Trainers and Supervisors 10.3.3.3. Supervision of CTP Supervisors 10.3.4. Training and …