WebCTEP RESOURCES Agent Management Cancer Trials Support Unit (CTSU) Central Institutional Review Board (CIRB) CTEP Forms, Templates and Documents CTEP … WebCTEP-AERS Transition Timeline • Training: – Began end of October 2013 and will continue as needed throughout 2014 and beyond – Standing trainings (3 per week) conducted beginning of December 2013 • Pilot: – October – December 2013 • CTEP-AERS open to full community for use in place of AdEERS for all relevant studies:

ALLIANCE FOR CLINICAL TRIALS IN ONCOLOGY ALLIANCE …

WebDec 15, 2012 · 1 result found containing all search terms. 45 results found containing some search terms. WebAn application for integrated clinical trials management and reporting, including Serious Adverse Event (SAE) reporting through the CTEP-Adverse Event Reporting System ( CTEP-AERS ), ordering of investigational agents, and trial monitoring/audits. Registration and Credentialing Repository (RCR) portfolio bonds

CTEP NCI Adverse Event Reporting Guidelines - National …

Weba baseline form that is not included in the Rave-CTEP-AERS integration. AEs that occur prior to enrollment must begin and end on the baseline Adverse Event form and should … WebRave write access; responsible for data management and uploads of Central Monitoring documents; and using Rave CTEP- AERS safety reporting tools. No. Yes. AP, NPIVR, IVR. Yes. No. 1. NA. Rave CRA. System. Rave Investigator. Investigator assigned to sign-off on the CRFs in Rave. No. No. ... Tasks Log Last modified by: Randall, Wayne (NIH/NCI) [C WebWe would like to show you a description here but the site won’t allow us. Request Provisional Access - National Institutes of Health portfolio book sizes