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Data Integrity in Clinical Trials in [Latest methods]

 
  September 28, 2018  
     
 
Netzealous LLC DBA - Compliance4All, Online
2018-11-16


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

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
 
 
Organized by: Event Manager
Invited Speakers:
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.
 
Deadline for Abstracts: 2018-11-15
 
Registration: https://www.compliance4all.com/control/w_product/~product_id=502172LIVE?channel=hum-molgen_Nov_2018_SEO
E-mail: support@compliance4All.com
 
 
   
 
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