Clinical Research Professional Certification Preparation and GCP Review Course (Nov, 2017)

Clinical Research Professional Certification Preparation and GCP Review Course is organized by Society of Clinical Research Associates (SOCRA) and would be held on Nov 13, 2017 at Simches Research Center, Boston, Massachusetts, United States Of America.

This CME Conference has been approved with a maximum of 6.5 Continuing Education Credits.

Conference Objectives are :
• Discuss the basic requirements necessary to meet the demands of a CRP in clinical practice
• Discuss the basic components of compliance - Law, regulation, guidance, policy and procedure
• Explain the drug/biologic development process
• Describe the device development process
• Outline concepts for Good Clinical Practice (GCP)
• Explain the elements of informed consent
• Describe the membership and reporting requirements of IRBs
• Explain rules relating to financial disclosure
• Discuss the basics of study design
• Explain the rules and reporting requirements for adverse events and serious adverse events
• Explain study closure procedures and record retention guidelines
• Outline the reasons for monitoring, audits and site visits
• Explain the Food and Drug Administration rules, regulations, and guidelines on research
• Discuss the importance of investigational drug accountability
• Demonstrate and describe how to read clinical reports and records
• Discuss Quality Assurance including, Monitoring and Auditing
•Explain issues that would constitute clinical fraud

Additional details will be posted as soon as they are available.