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Effective Training Practices for FDA Compliance Usa 2017 webinar by Compliance4all

 
  November 17, 2016  
     
 
Compliance4All, Online
2017-01-26


Overview:
No or inadequate training of employees is one of most frequently cited 

deviations in FDA inspectional observations and warning letters. Trainings 

are either not planned, not conducted, not evaluated or not documented 

as expected by inspectors. 

Areas Covered in the Session:
    GxP training requirements in US and EU
    Most frequently cited deviations
    Developing an effective training program for a company, site or 

department.

Who Will Benefit:
    Training departments
    QA managers and personnel
    Analysts and lab managers
    Validation specialists
    Regulatory affairs
    Human resources (HR) managers and staff
    Documentation department
    Consultants




 
 
Organized by: Compliance4All
Invited Speakers:
Speaker Profile:
Dr. Ludwig Huber Ph.D., is the director and editor of Labcompliance the 

global online resource for validation and compliance. He is the author of 

the books "Validation and Qualification in Analytical Laboratories" and 

"Validation of Computerized Analytical and Networked Systems, Informa 

Healthcare".
 
Deadline for Abstracts: 2017-01-25
 
Registration:
Contact Detail:

Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com
http://www.compliance4all.com/
Twitter Follow us – https://twitter.com/compliance4all
Facebook Like us – https://www.facebook.com/Compliance4all
LinkedIn Like us – https://www.linkedin.com/company/compliance4all
E-mail: support@compliance4All.com
 
   
 
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