Data Integrity in Clinical Trials in [Latest methods]

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Category GMP Data Integrity, Quality Trainings, data integrity pharmaceutical, mhra data integrity, data integrity audit checklist, data integrity guidance, Quality Operations Managers

Deadline: November 14, 2018 | Date: November 16, 2018

Venue/Country: Online, U.S.A

Updated: 2018-09-07 15:33:57 (GMT+9)

Call For Papers - CFP

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: supportcompliance4All.com