Data Integrity in Clinical Trials in [Latest methods]

Overview:The clinical data recording process, however, as inspected/audited by inspectors/auditors is initiated with the recorded data, either in the Case Report Form, or in some other system, or in an electronic database.
Why should you Attend:This course has been planned to provide you with understanding of Principles of Research Data Integrity and the essential skills and tools to evaluate the potential impact of compromised data integrity.
Areas Covered in the Session:Principles of Research Data IntegrityPotential impact of compromised data integrityDetecting issues with clinical data quality and integrityQA supports for data integrity and quality
Who Will Benefit:Clinical Monitors, Study Nurses and InvestigatorsValidation ManagersQA Managers, Project ManagersData Managers and Statisticians
Speaker Profile:Amer Alghabban is currently the Managing Director of GxP Compliance and Training Partners (GCTP) helping pharmaceutical companies to achieve compliance with GCP, GVP, GCLP and GLP. Amer has over 27 years’ experience in the pharmaceutical industry.
Event Fee: One Dial-in One Attendee Price: US $290.00
Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: support@compliance4All.com