3-Hour Virtual Seminar Data Integrity in Clinical Trials
WebcastFaculty
OVERVIEW
3-Hour Virtual Seminar Data Integrity in Clinical Trials is organized by Compliance4All and will be held on Nov 16, 2018.
Overview:
Clinical trials' data gives an accurate representation of what we measure to evaluate effects of the treatments under comparison. 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 Integrity
• Potential impact of compromised data integrity
• Detecting issues with clinical data quality and integrity
• QA supports for data integrity and quality
Who Will Benefit:
• Employees involved in Designing, Conducting, Evaluating, and Documenting of Clinical Trials
• Clinical Monitors, Study Nurses and Investigators
• Validation Managers
• QA Managers, Project Managers
• Data Managers and Statisticians
• Pharmaceutical Companies, Sponsors, Contractors (for example CROs, analytical labs) and Vendors for Electronic Systems (including hosting partner)
• Inspectors Responsible for Performing GCP Inspections and Needing to understand and Assess Data Integrity
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
Overview:
Clinical trials' data gives an accurate representation of what we measure to evaluate effects of the treatments under comparison. 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 Integrity
• Potential impact of compromised data integrity
• Detecting issues with clinical data quality and integrity
• QA supports for data integrity and quality
Who Will Benefit:
• Employees involved in Designing, Conducting, Evaluating, and Documenting of Clinical Trials
• Clinical Monitors, Study Nurses and Investigators
• Validation Managers
• QA Managers, Project Managers
• Data Managers and Statisticians
• Pharmaceutical Companies, Sponsors, Contractors (for example CROs, analytical labs) and Vendors for Electronic Systems (including hosting partner)
• Inspectors Responsible for Performing GCP Inspections and Needing to understand and Assess Data Integrity
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
SPECIALITIES
Health InformaticsMedical Education
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