Data Integrity in Clinical Trials in [Latest methods]

  • 290.00 Dollar US$
  • Published date: September 12, 2018
    • Fremont, California, United States

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 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:
Clinical Monitors, Study Nurses and Investigators
Validation Managers
QA Managers, Project Managers
Data 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: +1-800-447-9407
Email: support@compliance4All.com

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