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CRA eCOURSE OUTLINE
LESSON 1
· WHAT IS A CLINICAL TRIAL? (Clinical Study)
· WHAT IS A CRA? WHO CAN BE A CRA?
· ABOUT THE e-BOOK - Definitive Guide For The Clinical Research Associate
LESSON 2
· PHARMACEUTICAL INDUSTRY AND THE DRUG DEVELOPMENT PROCESS.
· COMPLEX CLINICAL RESEARCH REGULATIONS, WHY?
LESSON 3
· INDEPENDENT ETHICS COMMITTEE (IEC) INSTITUTIONAL REVIEW BOARD (IRB) PROCESS
LESSON 4
· THE INFORMED CONSENT
LESSON 5
· INVESTIGATOR SITE SELECTION AND QUALIFICATION VISITS
LESSON 6
· SITE INITIATION - PREPARATION & VISITS
LESSON 7
· MONITORING INVESTIGATIONAL SITES
LESSON 8
· ADVERSE EVENTS & SAFETY MONITORING
LESSON 9
· STUDY TERMINATION VISITS
LESSON 10
· THE STUDY PROTOCOL
· ELECTRONIC DATA CAPTURE in clinical research
· PATIENT RETENTION & COMPLIANCE
NOTE: Lessons 1 to 3 are available to all registered members while Lessons 4 to 10 are available to only registered members that have subscribed to the CRA eBook for at least 15 months.
You will need a password to access lessons 4 to 10.
CLICK HERE TO DOWNLOAD YOUR FREE SAMPLE OF THE eBOOK
