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How to plan risk based approaches for clinical trials

  December 05, 2017  
Netzealous LLC DBA - Compliance4All, Online

You will understand how to identify, evaluate and also how to 

implement specific risk based techniques for risk management used in 

clinical trials.

Areas Covered in the Session:
Have explained key risk based process/tools and techniques
Review a risk based approach to protocol design
Understand risk based approach to monitoring / data handling
Review of risk based approaches to QC / QA (Auditing)
Hear best practice of these new risk requirements

Who Will Benefit:
Clinical Development Managers and Personnel
Clinical Research Associates
Clinical Research Archiving and Document Management Personnel
Quality Assurance Managers and Auditors
Clinical Development Managers and Personnel

Event Fee: One Dial-in One Attendee Price: US$150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com
Organized by: Compliance4All
Invited Speakers:
Speaker Profile:
Dr. Laura Brown , PhD, MBA, Diploma Clinical Sciences, is an 

independent QA and training consultant in the pharmaceutical industry. 

She is a managing director with LB Training and Development Ltd., 

course director for the M.Sc. in Clinical Research, School of Pharmacy 

at the University of Cardiff, and course director for M.Sc. Regulatory 

Affairs, TOPRA. Dr. Brown has 20 years experience running clinical 

trials and clinical quality assurance in the pharmaceutical industry, and 

auditing clinical trials internationally.
Deadline for Abstracts: 2018-02-11

Full Details & Registration Link:


E-mail: support@compliance4All.com
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