Data Integrity in Clinical Trials in [Latest methods]

MessageThis Webinar is over
Date Nov 16, 2018
Time 09:00 AM to 12:00 PM
Cost 290.00
Online
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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