Clinical Research fast track, Scottsdale, AZ, 12/21, Trained and learned common type of clinical trial, clinical research ethics, Laboratory and pre-clinical research, phases of clinical trial, history of clinical research in human subjects., Learned and practiced activities about ICH GCP E6 (R2) Good clinical practice, 13 principles of ICH GCP E6 (R2)., Investigator responsibilities, informed consent IC, HIPAA authorization, Code of federal regulation CFR., Sponsor responsibilities SO, Institutional Review board IRB, Regulatory binder, FDA 1572, DOA., Training log, PIB, Protocol, Trial budgeting, sections of the protocol, ALOCA-C principles, and additions., CFR, IWRS, Data collection, CFR, ECRF, Lab portal, clinical trial management system., Subjects’ retention & recruitments., Importance of adverse events AE and severe adverse events SAV documentation, protocol deviation, and violation along with tips for prevention of deviation, FDA form 483, role of monitor (CRA)., Research skills training including Blood pressure, proper documentation of trial procedure, learned., How to take/perform Heart rate, Electrocardiogram, centrifuge, venipunctures, pregnancy test, and urinalysis handling, learned about the errors in trial procedures and prevention.